2-216237112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237112
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237112
    reference: chr 2
allele count: 2
allele frequency: 1.662427476601333e-5
allele num: 120306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.5705-14C>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.5705-14C>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.5705-89C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.332-89C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000461974
  gene symbol: FN1
  hgvsc: ENST00000461974.1:n.94C>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.5975-374C>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.5978-374C>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.5974+933C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2126-14C>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.5975-14C>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.6248-14C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000485567
  gene symbol: FN1
  hgvsc: ENST00000485567.1:n.51C>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.5705-374C>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.5975-89C>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.5975-14C>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.6248-14C>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.5975-374C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7385-14C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.368-89C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-216237116-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237116
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237116
    reference: chr 2
allele count: 2
allele frequency: 1.663174001264012e-5
allele num: 120252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.5975-378C>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.5705-18C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7385-18C>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.5975-18C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000461974
  gene symbol: FN1
  hgvsc: ENST00000461974.1:n.90C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000485567
  gene symbol: FN1
  hgvsc: ENST00000485567.1:n.47C>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.5975-378C>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.5975-18C>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.5705-93C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2126-18C>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.5975-93C>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.5974+929C>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.6248-18C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.368-93C>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.5978-378C>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.5705-18C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.332-93C>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.6248-18C>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.5705-378C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS

2-216237133-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237133
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237133
    reference: chr 2
allele count: 1
allele frequency: 8.34640937468701e-6
allele num: 119812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.368-110G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7385-35G>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.5975-35G>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.5978-395G>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.5705-395G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000461974
  gene symbol: FN1
  hgvsc: ENST00000461974.1:n.73G>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.6248-35G>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.5975-35G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2126-35G>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.5975-395G>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.5974+912G>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.5975-395G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000485567
  gene symbol: FN1
  hgvsc: ENST00000485567.1:n.30G>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.5705-35G>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.6248-35G>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.5705-110G>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.5975-110G>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.5705-35G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.332-110G>A
  variant of: http://identifiers.org/hgnc/3778
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

2-216237134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237134
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237134
    reference: chr 2
allele count: 1
allele frequency: 8.352683717278361e-6
allele num: 119722
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.5975-396C>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.6248-36C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000461974
  gene symbol: FN1
  hgvsc: ENST00000461974.1:n.72C>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.5974+911C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2126-36C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000485567
  gene symbol: FN1
  hgvsc: ENST00000485567.1:n.29C>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.6248-36C>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.5705-36C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.332-111C>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.5975-36C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7385-36C>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.5705-396C>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.5975-396C>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.5705-111C>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.5978-396C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.368-111C>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.5975-111C>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.5705-36C>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.5975-36C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

2-216237136-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237136
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237136
    reference: chr 2
allele count: 1
allele frequency: 8.355614973262032e-6
allele num: 119680
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.5975-113T>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.5975-398T>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.5975-38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.332-113T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2126-38T>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.5974+909T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7385-38T>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.5978-398T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000461974
  gene symbol: FN1
  hgvsc: ENST00000461974.1:n.70T>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.5705-38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000485567
  gene symbol: FN1
  hgvsc: ENST00000485567.1:n.27T>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.5705-398T>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.5975-398T>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.6248-38T>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.5705-38T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.368-113T>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.5975-38T>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.6248-38T>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.5705-113T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15537
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

2-216237136-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237136
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237136
    reference: chr 2
allele count: 1
allele frequency: 8.355614973262032e-6
allele num: 119680
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.5705-398T>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.5705-113T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.332-113T>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.5974+909T>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.5705-38T>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.5975-398T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2126-38T>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.5975-38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000461974
  gene symbol: FN1
  hgvsc: ENST00000461974.1:n.70T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000485567
  gene symbol: FN1
  hgvsc: ENST00000485567.1:n.27T>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.5975-113T>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.5705-38T>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.6248-38T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.368-113T>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.5978-398T>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.5975-398T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7385-38T>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.5975-38T>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.6248-38T>A
  variant of: http://identifiers.org/hgnc/3778
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

2-216237144-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237144
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237144
    reference: chr 2
allele count: 4
allele frequency: 3.356324153786773e-5
allele num: 119178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.5978-406G>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.5975-121G>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.5705-406G>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.5975-406G>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.6248-46G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2126-46G>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.5975-46G>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.5974+901G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.332-121G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000461974
  gene symbol: FN1
  hgvsc: ENST00000461974.1:n.62G>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.6248-46G>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.5705-121G>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.5975-406G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000485567
  gene symbol: FN1
  hgvsc: ENST00000485567.1:n.19G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.368-121G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7385-46G>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.5705-46G>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.5975-46G>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.5705-46G>A
  variant of: http://identifiers.org/hgnc/3778
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

2-216237994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216237994
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216237994
    reference: chr 2
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.5974+51C>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.6247+51C>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.5974+51C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+51C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+51C>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.5974+51C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+51C>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.5974+51C>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.5974+51C>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.5704+51C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+51C>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.5974+51C>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.5704+51C>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.6247+51C>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.5704+51C>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.5704+51C>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.5977+51C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

2-216238001-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238001
    reference: chr 2
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
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.5704+44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+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.5704+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.5974+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.6247+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.5974+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.5704+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.5974+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.5704+44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+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.6247+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.5977+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.5974+44C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+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.5974+44C>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.5974+44C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

2-216238002-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238002
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238002
    reference: chr 2
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.6247+43A>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.5704+43A>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.5974+43A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+43A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+43A>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.6247+43A>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.5977+43A>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.5974+43A>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.5704+43A>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.5704+43A>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.5974+43A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+43A>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.5974+43A>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+43A>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.5704+43A>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.5974+43A>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.5974+43A>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5583
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-216238008-CCTAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238008
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238004
    reference: chr 2
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+33_331+36delATAG
  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.5974+33_5974+36delATAG
  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.5974+33_5974+36delATAG
  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.5704+33_5704+36delATAG
  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.5974+33_5974+36delATAG
  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.5704+33_5704+36delATAG
  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.5704+33_5704+36delATAG
  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.6247+33_6247+36delATAG
  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.5974+33_5974+36delATAG
  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.5704+33_5704+36delATAG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+33_367+36delATAG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+33_7384+36delATAG
  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.5977+33_5977+36delATAG
  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.5974+33_5974+36delATAG
  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.6247+33_6247+36delATAG
  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.5974+33_5974+36delATAG
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+33_2125+36delATAG
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4670
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: CCTAT
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

2-216238011-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238011
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238011
    reference: chr 2
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5974+34T>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.5704+34T>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.5974+34T>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.5704+34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+34T>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.6247+34T>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.5704+34T>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.5704+34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+34T>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.6247+34T>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.5974+34T>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.5977+34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+34T>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.5974+34T>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.5974+34T>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.5974+34T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4669
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP

2-216238011-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238011
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238011
    reference: chr 2
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.6247+34T>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.5974+34T>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.5977+34T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+34T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+34T>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.5974+34T>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.5704+34T>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.5704+34T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+34T>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.5704+34T>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.6247+34T>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.5974+34T>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.5704+34T>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.5974+34T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+34T>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.5974+34T>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.5974+34T>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6791
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-216238013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238013
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238013
    reference: chr 2
allele count: 50
allele frequency: 4.119634176485128e-4
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+32G>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.5974+32G>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.5704+32G>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.5974+32G>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.5704+32G>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.6247+32G>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.5974+32G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+32G>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.5974+32G>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.5977+32G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+32G>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.5704+32G>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.6247+32G>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.5704+32G>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.5974+32G>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.5974+32G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+32G>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

2-216238028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238028
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238028
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.6247+17G>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.5704+17G>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.5974+17G>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.5974+17G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+17G>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.5974+17G>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.5977+17G>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.5704+17G>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.5974+17G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+17G>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.5704+17G>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.5974+17G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+17G>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.5974+17G>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.5704+17G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+17G>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.6247+17G>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

2-216238031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238031
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238031
    reference: chr 2
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.6247+14G>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.5974+14G>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.5977+14G>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.5974+14G>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.5704+14G>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.5704+14G>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.5974+14G>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.5974+14G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+14G>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.5974+14G>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.5704+14G>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.6247+14G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+14G>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.5974+14G>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.5704+14G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+14G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+14G>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

2-216238035-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238035
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238035
    reference: chr 2
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+10T>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.5704+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.6247+10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+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.5704+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.5974+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.5704+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.5974+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.5974+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.5974+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.5704+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.5977+10T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+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.6247+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.5974+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.5974+10T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

2-216238037-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238037
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238037
    reference: chr 2
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
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.5704+8T>A
  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.5704+8T>A
  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.5977+8T>A
  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.5974+8T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+8T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+8T>A
  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.5704+8T>A
  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.5974+8T>A
  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.5974+8T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+8T>A
  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.5974+8T>A
  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.5974+8T>A
  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.5974+8T>A
  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.5704+8T>A
  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.6247+8T>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+8T>A
  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.6247+8T>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6247+8T>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

2-216238042-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238042
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238042
    reference: chr 2
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
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.5974+3A>G
  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.5974+3A>G
  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.5974+3A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.367+3A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.331+3A>G
  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.5974+3A>G
  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.5974+3A>G
  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.5704+3A>G
  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.5704+3A>G
  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.6247+3A>G
  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.5704+3A>G
  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.5704+3A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7384+3A>G
  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.6247+3A>G
  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.5977+3A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2125+3A>G
  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.5974+3A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6247+3A>G
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

2-216238050-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238050
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238050
    reference: chr 2
allele count: 7
allele frequency: 5.765682656826568e-5
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.5969A>C
  hgvsp: ENSP00000352696.1:p.Lys1990Thr
  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.5969A>C
  hgvsp: ENSP00000338200.4:p.Lys1990Thr
  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.5969A>C
  hgvsp: ENSP00000273049.7:p.Lys1990Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.326A>C
  hgvsp: ENSP00000392565.1:p.Lys109Thr
  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.5699A>C
  hgvsp: ENSP00000415018.1:p.Lys1900Thr
  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.5969A>C
  hgvsp: ENSP00000410422.1:p.Lys1990Thr
  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.5699A>C
  hgvsp: ENSP00000394423.1:p.Lys1900Thr
  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.6242A>C
  hgvsp: ENSP00000346839.4:p.Lys2081Thr
  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.5699A>C
  hgvsp: ENSP00000348285.4:p.Lys1900Thr
  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.6242A>C
  hgvsp: ENSP00000323534.6:p.Lys2081Thr
  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.5972A>C
  hgvsp: ENSP00000399538.2:p.Lys1991Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.362A>C
  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.5969A>C
  hgvsp: ENSP00000265312.6:p.Lys1990Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2120A>C
  hgvsp: ENSP00000416139.1:p.Lys707Thr
  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.5969A>C
  hgvsp: ENSP00000349509.2:p.Lys1990Thr
  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.5699A>C
  hgvsp: ENSP00000350534.4:p.Lys1900Thr
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7379A>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys2081Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

2-216238055-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238055
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238055
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.5694G>A
  hgvsp: ENST00000357867.4:c.5694G>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.6237G>A
  hgvsp: ENST00000354785.4:c.6237G>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.5964G>A
  hgvsp: ENST00000345488.5:c.5964G>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.6237G>A
  hgvsp: ENST00000323926.6:c.6237G>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.5964G>A
  hgvsp: ENST00000359671.1:c.5964G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2115G>A
  hgvsp: ENST00000456923.1:c.2115G>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.5694G>A
  hgvsp: ENST00000356005.4:c.5694G>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.5964G>A
  hgvsp: ENST00000336916.4:c.5964G>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.5967G>A
  hgvsp: ENST00000432072.2:c.5967G>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.5694G>A
  hgvsp: ENST00000443816.1:c.5694G>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.5964G>A
  hgvsp: ENST00000346544.3:c.5964G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.357G>A
  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.5694G>A
  hgvsp: ENST00000421182.1:c.5694G>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.5964G>A
  hgvsp: ENST00000357009.2:c.5964G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7374G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.321G>A
  hgvsp: ENST00000438981.1:c.321G>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.5964G>A
  hgvsp: ENST00000446046.1:c.5964G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg2079Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

2-216238057-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238057
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238057
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5962A>C
  hgvsp: ENST00000345488.5:c.5962A>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.5692A>C
  hgvsp: ENST00000356005.4:c.5692A>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.5962A>C
  hgvsp: ENST00000357009.2:c.5962A>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.5962A>C
  hgvsp: ENST00000359671.1:c.5962A>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.6235A>C
  hgvsp: ENST00000323926.6:c.6235A>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.5962A>C
  hgvsp: ENST00000346544.3:c.5962A>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.5962A>C
  hgvsp: ENST00000336916.4:c.5962A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2113A>C
  hgvsp: ENST00000456923.1:c.2113A>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.5692A>C
  hgvsp: ENST00000443816.1:c.5692A>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.5965A>C
  hgvsp: ENST00000432072.2:c.5965A>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.5962A>C
  hgvsp: ENST00000446046.1:c.5962A>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.6235A>C
  hgvsp: ENST00000354785.4:c.6235A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.319A>C
  hgvsp: ENST00000438981.1:c.319A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.355A>C
  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.5692A>C
  hgvsp: ENST00000421182.1:c.5692A>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.5692A>C
  hgvsp: ENST00000357867.4:c.5692A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7372A>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg2079Arg
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

2-216238063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238063
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238063
    reference: chr 2
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.5686A>G
  hgvsp: ENSP00000348285.4:p.Ile1896Val
  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.5686A>G
  hgvsp: ENSP00000415018.1:p.Ile1896Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7366A>G
  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.5956A>G
  hgvsp: ENSP00000338200.4:p.Ile1986Val
  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.6229A>G
  hgvsp: ENSP00000323534.6:p.Ile2077Val
  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.6229A>G
  hgvsp: ENSP00000346839.4:p.Ile2077Val
  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.5956A>G
  hgvsp: ENSP00000349509.2:p.Ile1986Val
  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.5956A>G
  hgvsp: ENSP00000273049.7:p.Ile1986Val
  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.5956A>G
  hgvsp: ENSP00000352696.1:p.Ile1986Val
  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.5959A>G
  hgvsp: ENSP00000399538.2:p.Ile1987Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.313A>G
  hgvsp: ENSP00000392565.1:p.Ile105Val
  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.5686A>G
  hgvsp: ENSP00000350534.4:p.Ile1896Val
  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.5686A>G
  hgvsp: ENSP00000394423.1:p.Ile1896Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.349A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2107A>G
  hgvsp: ENSP00000416139.1:p.Ile703Val
  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.5956A>G
  hgvsp: ENSP00000265312.6:p.Ile1986Val
  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.5956A>G
  hgvsp: ENSP00000410422.1:p.Ile1986Val
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile2077Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

2-216238068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238068
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238068
    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: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5951C>T
  hgvsp: ENSP00000273049.7:p.Pro1984Leu
  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.5681C>T
  hgvsp: ENSP00000348285.4:p.Pro1894Leu
  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.5951C>T
  hgvsp: ENSP00000338200.4:p.Pro1984Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7361C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.308C>T
  hgvsp: ENSP00000392565.1:p.Pro103Leu
  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.5681C>T
  hgvsp: ENSP00000394423.1:p.Pro1894Leu
  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.6224C>T
  hgvsp: ENSP00000346839.4:p.Pro2075Leu
  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.5951C>T
  hgvsp: ENSP00000352696.1:p.Pro1984Leu
  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.5951C>T
  hgvsp: ENSP00000265312.6:p.Pro1984Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2102C>T
  hgvsp: ENSP00000416139.1:p.Pro701Leu
  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.5681C>T
  hgvsp: ENSP00000415018.1:p.Pro1894Leu
  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.5954C>T
  hgvsp: ENSP00000399538.2:p.Pro1985Leu
  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.5681C>T
  hgvsp: ENSP00000350534.4:p.Pro1894Leu
  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.5951C>T
  hgvsp: ENSP00000410422.1:p.Pro1984Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.344C>T
  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.6224C>T
  hgvsp: ENSP00000323534.6:p.Pro2075Leu
  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.5951C>T
  hgvsp: ENSP00000349509.2:p.Pro1984Leu
  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: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro2075Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

2-216238073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238073
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238073
    reference: chr 2
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
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.6219C>T
  hgvsp: ENST00000323926.6:c.6219C>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.5946C>T
  hgvsp: ENST00000345488.5:c.5946C>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.5676C>T
  hgvsp: ENST00000443816.1:c.5676C>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.5946C>T
  hgvsp: ENST00000446046.1:c.5946C>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.5676C>T
  hgvsp: ENST00000421182.1:c.5676C>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.5676C>T
  hgvsp: ENST00000356005.4:c.5676C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.339C>T
  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.6219C>T
  hgvsp: ENST00000354785.4:c.6219C>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.5946C>T
  hgvsp: ENST00000357009.2:c.5946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.303C>T
  hgvsp: ENST00000438981.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2097C>T
  hgvsp: ENST00000456923.1:c.2097C>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.5946C>T
  hgvsp: ENST00000346544.3:c.5946C>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.5946C>T
  hgvsp: ENST00000359671.1:c.5946C>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.5676C>T
  hgvsp: ENST00000357867.4:c.5676C>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.5949C>T
  hgvsp: ENST00000432072.2:c.5949C>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.5946C>T
  hgvsp: ENST00000336916.4:c.5946C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7356C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser2073Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff

2-216238083-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238083
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238083
    reference: chr 2
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.5936A>G
  hgvsp: ENSP00000265312.6:p.Asn1979Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7346A>G
  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.5666A>G
  hgvsp: ENSP00000394423.1:p.Asn1889Ser
  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.5936A>G
  hgvsp: ENSP00000349509.2:p.Asn1979Ser
  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.5936A>G
  hgvsp: ENSP00000273049.7:p.Asn1979Ser
  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.5666A>G
  hgvsp: ENSP00000348285.4:p.Asn1889Ser
  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.5666A>G
  hgvsp: ENSP00000350534.4:p.Asn1889Ser
  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.6209A>G
  hgvsp: ENSP00000346839.4:p.Asn2070Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.293A>G
  hgvsp: ENSP00000392565.1:p.Asn98Ser
  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.5666A>G
  hgvsp: ENSP00000415018.1:p.Asn1889Ser
  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.5936A>G
  hgvsp: ENSP00000410422.1:p.Asn1979Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.329A>G
  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.6209A>G
  hgvsp: ENSP00000323534.6:p.Asn2070Ser
  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.5936A>G
  hgvsp: ENSP00000338200.4:p.Asn1979Ser
  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.5936A>G
  hgvsp: ENSP00000352696.1:p.Asn1979Ser
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2087A>G
  hgvsp: ENSP00000416139.1:p.Asn696Ser
  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.5939A>G
  hgvsp: ENSP00000399538.2:p.Asn1980Ser
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn2070Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

2-216238100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238100
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238100
    reference: chr 2
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
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.5919C>T
  hgvsp: ENST00000357009.2:c.5919C>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.5919C>T
  hgvsp: ENST00000359671.1:c.5919C>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.5649C>T
  hgvsp: ENST00000357867.4:c.5649C>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.5649C>T
  hgvsp: ENST00000356005.4:c.5649C>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.5919C>T
  hgvsp: ENST00000446046.1:c.5919C>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.5919C>T
  hgvsp: ENST00000346544.3:c.5919C>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.6192C>T
  hgvsp: ENST00000323926.6:c.6192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2070C>T
  hgvsp: ENST00000456923.1:c.2070C>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.5649C>T
  hgvsp: ENST00000421182.1:c.5649C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7329C>T
  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.5919C>T
  hgvsp: ENST00000345488.5:c.5919C>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.5649C>T
  hgvsp: ENST00000443816.1:c.5649C>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.5922C>T
  hgvsp: ENST00000432072.2:c.5922C>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.6192C>T
  hgvsp: ENST00000354785.4:c.6192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.276C>T
  hgvsp: ENST00000438981.1:c.276C>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.5919C>T
  hgvsp: ENST00000336916.4:c.5919C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.312C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val2064Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD

2-216238108-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238108
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238108
    reference: chr 2
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.5911A>G
  hgvsp: ENSP00000265312.6:p.Ile1971Val
  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.5641A>G
  hgvsp: ENSP00000394423.1:p.Ile1881Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.304A>G
  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.6184A>G
  hgvsp: ENSP00000346839.4:p.Ile2062Val
  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.5911A>G
  hgvsp: ENSP00000349509.2:p.Ile1971Val
  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.5914A>G
  hgvsp: ENSP00000399538.2:p.Ile1972Val
  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.5641A>G
  hgvsp: ENSP00000350534.4:p.Ile1881Val
  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.6184A>G
  hgvsp: ENSP00000323534.6:p.Ile2062Val
  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.5641A>G
  hgvsp: ENSP00000348285.4:p.Ile1881Val
  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.5911A>G
  hgvsp: ENSP00000352696.1:p.Ile1971Val
  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.5641A>G
  hgvsp: ENSP00000415018.1:p.Ile1881Val
  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.5911A>G
  hgvsp: ENSP00000338200.4:p.Ile1971Val
  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.5911A>G
  hgvsp: ENSP00000273049.7:p.Ile1971Val
  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.5911A>G
  hgvsp: ENSP00000410422.1:p.Ile1971Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2062A>G
  hgvsp: ENSP00000416139.1:p.Ile688Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7321A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.268A>G
  hgvsp: ENSP00000392565.1:p.Ile90Val
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile2062Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-216238117-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238117
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238117
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
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.5902G>A
  hgvsp: ENSP00000352696.1:p.Glu1968Lys
  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.5632G>A
  hgvsp: ENSP00000394423.1:p.Glu1878Lys
  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.5902G>A
  hgvsp: ENSP00000410422.1:p.Glu1968Lys
  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.5902G>A
  hgvsp: ENSP00000273049.7:p.Glu1968Lys
  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.5632G>A
  hgvsp: ENSP00000415018.1:p.Glu1878Lys
  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.6175G>A
  hgvsp: ENSP00000323534.6:p.Glu2059Lys
  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.5632G>A
  hgvsp: ENSP00000348285.4:p.Glu1878Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.295G>A
  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.5632G>A
  hgvsp: ENSP00000350534.4:p.Glu1878Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7312G>A
  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.6175G>A
  hgvsp: ENSP00000346839.4:p.Glu2059Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.259G>A
  hgvsp: ENSP00000392565.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2053G>A
  hgvsp: ENSP00000416139.1:p.Glu685Lys
  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.5902G>A
  hgvsp: ENSP00000349509.2:p.Glu1968Lys
  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.5902G>A
  hgvsp: ENSP00000338200.4:p.Glu1968Lys
  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.5902G>A
  hgvsp: ENSP00000265312.6:p.Glu1968Lys
  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.5905G>A
  hgvsp: ENSP00000399538.2:p.Glu1969Lys
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7252
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu2059Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

2-216238118-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238118
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238118
    reference: chr 2
allele count: 6
allele frequency: 4.942257952916756e-5
allele num: 121402
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.5901C>T
  hgvsp: ENST00000346544.3:c.5901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.294C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7311C>T
  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.5904C>T
  hgvsp: ENST00000432072.2:c.5904C>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.5631C>T
  hgvsp: ENST00000357867.4:c.5631C>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.5901C>T
  hgvsp: ENST00000357009.2:c.5901C>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.5631C>T
  hgvsp: ENST00000356005.4:c.5631C>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.5631C>T
  hgvsp: ENST00000443816.1:c.5631C>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.5901C>T
  hgvsp: ENST00000446046.1:c.5901C>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.6174C>T
  hgvsp: ENST00000354785.4:c.6174C>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.6174C>T
  hgvsp: ENST00000323926.6:c.6174C>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.5901C>T
  hgvsp: ENST00000336916.4:c.5901C>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.5901C>T
  hgvsp: ENST00000345488.5:c.5901C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2052C>T
  hgvsp: ENST00000456923.1:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.258C>T
  hgvsp: ENST00000438981.1:c.258C>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.5901C>T
  hgvsp: ENST00000359671.1:c.5901C>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.5631C>T
  hgvsp: ENST00000421182.1:c.5631C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr2058Thr
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

2-216238119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238119
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238119
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.5630C>T
  hgvsp: ENSP00000348285.4:p.Thr1877Ile
  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.6173C>T
  hgvsp: ENSP00000323534.6:p.Thr2058Ile
  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.5900C>T
  hgvsp: ENSP00000349509.2:p.Thr1967Ile
  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.5900C>T
  hgvsp: ENSP00000273049.7:p.Thr1967Ile
  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.5630C>T
  hgvsp: ENSP00000350534.4:p.Thr1877Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.293C>T
  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.6173C>T
  hgvsp: ENSP00000346839.4:p.Thr2058Ile
  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.5630C>T
  hgvsp: ENSP00000415018.1:p.Thr1877Ile
  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.5630C>T
  hgvsp: ENSP00000394423.1:p.Thr1877Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.257C>T
  hgvsp: ENSP00000392565.1:p.Thr86Ile
  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.5900C>T
  hgvsp: ENSP00000352696.1:p.Thr1967Ile
  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.5900C>T
  hgvsp: ENSP00000338200.4:p.Thr1967Ile
  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.5900C>T
  hgvsp: ENSP00000410422.1:p.Thr1967Ile
  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.5903C>T
  hgvsp: ENSP00000399538.2:p.Thr1968Ile
  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.5900C>T
  hgvsp: ENSP00000265312.6:p.Thr1967Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2051C>T
  hgvsp: ENSP00000416139.1:p.Thr684Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7310C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr2058Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-216238122-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238122
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238122
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.5897G>T
  hgvsp: ENSP00000338200.4:p.Gly1966Val
  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.5627G>T
  hgvsp: ENSP00000394423.1:p.Gly1876Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2048G>T
  hgvsp: ENSP00000416139.1:p.Gly683Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7307G>T
  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.5627G>T
  hgvsp: ENSP00000348285.4:p.Gly1876Val
  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.5897G>T
  hgvsp: ENSP00000273049.7:p.Gly1966Val
  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.5627G>T
  hgvsp: ENSP00000350534.4:p.Gly1876Val
  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.6170G>T
  hgvsp: ENSP00000323534.6:p.Gly2057Val
  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.5897G>T
  hgvsp: ENSP00000265312.6:p.Gly1966Val
  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.5897G>T
  hgvsp: ENSP00000352696.1:p.Gly1966Val
  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.5897G>T
  hgvsp: ENSP00000410422.1:p.Gly1966Val
  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.5900G>T
  hgvsp: ENSP00000399538.2:p.Gly1967Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.290G>T
  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.6170G>T
  hgvsp: ENSP00000346839.4:p.Gly2057Val
  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.5897G>T
  hgvsp: ENSP00000349509.2:p.Gly1966Val
  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.5627G>T
  hgvsp: ENSP00000415018.1:p.Gly1876Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.254G>T
  hgvsp: ENSP00000392565.1:p.Gly85Val
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4665
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly2057Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-216238124-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238124
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238124
    reference: chr 2
allele count: 14
allele frequency: 1.153212520593081e-4
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.6168G>A
  hgvsp: ENST00000354785.4:c.6168G>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.5895G>A
  hgvsp: ENST00000345488.5:c.5895G>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.5625G>A
  hgvsp: ENST00000421182.1:c.5625G>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.6168G>A
  hgvsp: ENST00000323926.6:c.6168G>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.5895G>A
  hgvsp: ENST00000346544.3:c.5895G>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.5625G>A
  hgvsp: ENST00000357867.4:c.5625G>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.5898G>A
  hgvsp: ENST00000432072.2:c.5898G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7305G>A
  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.5895G>A
  hgvsp: ENST00000446046.1:c.5895G>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.5625G>A
  hgvsp: ENST00000443816.1:c.5625G>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.5895G>A
  hgvsp: ENST00000359671.1:c.5895G>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.5625G>A
  hgvsp: ENST00000356005.4:c.5625G>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.5895G>A
  hgvsp: ENST00000336916.4:c.5895G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.252G>A
  hgvsp: ENST00000438981.1:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.288G>A
  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.5895G>A
  hgvsp: ENST00000357009.2:c.5895G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2046G>A
  hgvsp: ENST00000456923.1:c.2046G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro2056Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-216238140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238140
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238140
    reference: chr 2
allele count: 4
allele frequency: 3.295327225993541e-5
allele num: 121384
alternate allele: A
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.5885-6C>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.5888-6C>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.5615-6C>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.6158-6C>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.5885-6C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-6C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-6C>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.5885-6C>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.5615-6C>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.5885-6C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-6C>T
  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.6158-6C>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.5615-6C>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.5885-6C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-6C>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.5615-6C>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.5885-6C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6158-6C>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS

2-216238140-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238140
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238140
    reference: chr 2
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
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.5885-6C>A
  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.6158-6C>A
  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.5615-6C>A
  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.5615-6C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-6C>A
  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.5885-6C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-6C>A
  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.5615-6C>A
  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.5885-6C>A
  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.5615-6C>A
  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.5885-6C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-6C>A
  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.5885-6C>A
  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.5885-6C>A
  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.6158-6C>A
  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.5888-6C>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-6C>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6787
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6158-6C>A
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

2-216238141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238141
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238141
    reference: chr 2
allele count: 10
allele frequency: 8.238182327451271e-5
allele num: 121386
alternate allele: A
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.5615-7C>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.6158-7C>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.5615-7C>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.5885-7C>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.5615-7C>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.5885-7C>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.5888-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-7C>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.5885-7C>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.5885-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-7C>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.5885-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.6158-7C>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.5885-7C>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.5615-7C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-7C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.6158-7C>T
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-216238143-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238143
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238143
    reference: chr 2
allele count: 3
allele frequency: 2.471454698235381e-5
allele num: 121386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.5615-9T>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.5885-9T>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.5885-9T>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-9T>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.5615-9T>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.5885-9T>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.5885-9T>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.6158-9T>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.5885-9T>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.5885-9T>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.6158-9T>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.5615-9T>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.5888-9T>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-9T>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-9T>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-9T>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.5615-9T>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

2-216238143-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238143
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238143
    reference: chr 2
allele count: 5
allele frequency: 4.119091163725636e-5
allele num: 121386
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.5615-9T>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.5888-9T>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.5615-9T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-9T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-9T>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.5885-9T>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.5615-9T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-9T>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.5615-9T>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.5885-9T>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.6158-9T>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.5885-9T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-9T>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.5885-9T>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.5885-9T>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.5885-9T>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.6158-9T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6783
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

2-216238144-G-GAAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238144
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238147
    reference: chr 2
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: GAAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-13_7295-11dupATT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-13_2036-11dupATT
  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.5615-13_5615-11dupATT
  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.5885-13_5885-11dupATT
  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.6158-13_6158-11dupATT
  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.5615-13_5615-11dupATT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-13_242-11dupATT
  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.6158-13_6158-11dupATT
  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.5885-13_5885-11dupATT
  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.5885-13_5885-11dupATT
  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.5615-13_5615-11dupATT
  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.5885-13_5885-11dupATT
  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.5885-13_5885-11dupATT
  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.5888-13_5888-11dupATT
  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.5885-13_5885-11dupATT
  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.5615-13_5615-11dupATT
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-13_278-11dupATT
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

2-216238147-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238147
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238147
    reference: chr 2
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.6158-13A>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.5888-13A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-13A>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.5615-13A>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.5615-13A>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.5615-13A>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.5885-13A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-13A>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.5885-13A>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.5885-13A>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.5885-13A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-13A>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.5615-13A>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.6158-13A>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.5885-13A>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.5885-13A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-13A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

2-216238163-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238163
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238163
    reference: chr 2
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.5888-29A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-29A>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.5885-29A>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.6158-29A>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.6158-29A>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.5615-29A>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.5885-29A>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.5615-29A>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.5885-29A>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.5615-29A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-29A>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.5885-29A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-29A>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.5885-29A>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.5615-29A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-29A>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.5885-29A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

2-216238168-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238168
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238168
    reference: chr 2
allele count: 106
allele frequency: 8.734056227546884e-4
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5885-34T>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.5615-34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-34T>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.6158-34T>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.5885-34T>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.5615-34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-34T>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.5885-34T>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.5885-34T>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.5885-34T>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.5615-34T>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.5615-34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-34T>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.6158-34T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-34T>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.5885-34T>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.5888-34T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5514
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

2-216238186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216238186
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216238186
    reference: chr 2
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5885-52C>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.6158-52C>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.5615-52C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.242-52C>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.5615-52C>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.5885-52C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7295-52C>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.5885-52C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.278-52C>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.5885-52C>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.5615-52C>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.5885-52C>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.6158-52C>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.5885-52C>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.5888-52C>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.5615-52C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2036-52C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

2-216239892-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239892
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239892
    reference: chr 2
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.5887+45A>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.6157+45A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+45A>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.5884+45A>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.5884+45A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+45A>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.5614+45A>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.5614+45A>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.5884+45A>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.5884+45A>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.5614+45A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+45A>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.5884+45A>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.5614+45A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+45A>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.6157+45A>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.5884+45A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-216239898-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239898
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239898
    reference: chr 2
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5884+39C>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.6157+39C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+39C>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.5884+39C>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.5614+39C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+39C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+39C>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.5614+39C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+39C>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.5884+39C>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.5884+39C>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.5614+39C>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.6157+39C>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.5614+39C>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.5887+39C>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.5884+39C>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.5884+39C>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7662
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

2-216239899-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239899
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239899
    reference: chr 2
allele count: 11
allele frequency: 9.066332586047738e-5
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.5614+38A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+38A>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.5884+38A>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.5884+38A>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.6157+38A>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.5887+38A>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.6157+38A>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.5884+38A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+38A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+38A>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.5884+38A>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.5614+38A>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.5614+38A>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.5884+38A>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.5884+38A>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.5614+38A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+38A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

2-216239901-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239901
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239901
    reference: chr 2
allele count: 3
allele frequency: 2.472310126582278e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.5614+36C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+36C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+36C>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.5884+36C>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.5884+36C>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.5887+36C>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.6157+36C>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.5884+36C>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.5614+36C>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.5884+36C>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.5884+36C>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.5884+36C>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.5614+36C>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.6157+36C>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.5614+36C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+36C>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+36C>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5154
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-216239902-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239902
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239902
    reference: chr 2
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.5614+35A>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.5887+35A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+35A>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.5884+35A>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.5614+35A>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.5884+35A>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.5884+35A>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.5884+35A>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.5614+35A>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.5884+35A>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.5884+35A>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.6157+35A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+35A>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.5614+35A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+35A>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.6157+35A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+35A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

2-216239906-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239906
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239906
    reference: chr 2
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5884+31T>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.5614+31T>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.5884+31T>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.5614+31T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+31T>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.5884+31T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+31T>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.5887+31T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+31T>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.5884+31T>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.5884+31T>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.6157+31T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+31T>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.5614+31T>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.5614+31T>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.6157+31T>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.5884+31T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

2-216239910-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239910
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239910
    reference: chr 2
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+27T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+27T>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.5884+27T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+27T>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.6157+27T>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.5884+27T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+27T>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.5614+27T>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.5884+27T>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.5884+27T>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.5614+27T>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.5884+27T>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.5884+27T>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.5614+27T>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.5887+27T>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.6157+27T>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.5614+27T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13427
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17712
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

2-216239917-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239917
    reference: chr 2
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
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.5884+20G>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.5884+20G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+20G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+20G>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.5884+20G>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.5614+20G>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.6157+20G>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.5614+20G>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.5884+20G>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.5884+20G>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.5614+20G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+20G>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.5887+20G>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.6157+20G>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.5884+20G>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.5614+20G>A
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+20G>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13428
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7666
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

2-216239922-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239922
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239922
    reference: chr 2
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5884+15A>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.5614+15A>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.5614+15A>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.5884+15A>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.5887+15A>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.6157+15A>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.5884+15A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+15A>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.5884+15A>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.5614+15A>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.5614+15A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+15A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+15A>G
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+15A>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.5884+15A>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.5884+15A>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.6157+15A>G
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-216239933-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239933
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239933
    reference: chr 2
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: G
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.6157+4T>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.5614+4T>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.5884+4T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2035+4T>C
  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.5884+4T>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.5614+4T>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.6157+4T>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.5884+4T>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.5884+4T>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.5884+4T>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.5614+4T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.241+4T>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.5884+4T>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.5887+4T>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.5614+4T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.277+4T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7294+4T>C
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.6157+4T>C
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-216239939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239939
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239939
    reference: chr 2
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.239C>T
  hgvsp: ENSP00000392565.1:p.Thr80Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000323534
  ensembl transcript: ENST00000323926
  gene symbol: FN1
  hgvsc: ENST00000323926.6:c.6155C>T
  hgvsp: ENSP00000323534.6:p.Thr2052Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000352696
  ensembl transcript: ENST00000359671
  gene symbol: FN1
  hgvsc: ENST00000359671.1:c.5882C>T
  hgvsp: ENSP00000352696.1:p.Thr1961Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5882C>T
  hgvsp: ENSP00000273049.7:p.Thr1961Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7292C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000394423
  ensembl transcript: ENST00000421182
  gene symbol: FN1
  hgvsc: ENST00000421182.1:c.5612C>T
  hgvsp: ENSP00000394423.1:p.Thr1871Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.5882C>T
  hgvsp: ENSP00000338200.4:p.Thr1961Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.5612C>T
  hgvsp: ENSP00000350534.4:p.Thr1871Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.5882C>T
  hgvsp: ENSP00000265312.6:p.Thr1961Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000346839
  ensembl transcript: ENST00000354785
  gene symbol: FN1
  hgvsc: ENST00000354785.4:c.6155C>T
  hgvsp: ENSP00000346839.4:p.Thr2052Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000348285
  ensembl transcript: ENST00000356005
  gene symbol: FN1
  hgvsc: ENST00000356005.4:c.5612C>T
  hgvsp: ENSP00000348285.4:p.Thr1871Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000410422
  ensembl transcript: ENST00000446046
  gene symbol: FN1
  hgvsc: ENST00000446046.1:c.5882C>T
  hgvsp: ENSP00000410422.1:p.Thr1961Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000399538
  ensembl transcript: ENST00000432072
  gene symbol: FN1
  hgvsc: ENST00000432072.2:c.5885C>T
  hgvsp: ENSP00000399538.2:p.Thr1962Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.275C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2033C>T
  hgvsp: ENSP00000416139.1:p.Thr678Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000415018
  ensembl transcript: ENST00000443816
  gene symbol: FN1
  hgvsc: ENST00000443816.1:c.5612C>T
  hgvsp: ENSP00000415018.1:p.Thr1871Ile
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.5882C>T
  hgvsp: ENSP00000349509.2:p.Thr1961Ile
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr2052Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/2-216239960-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239960
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239960
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000350534
  ensembl transcript: ENST00000357867
  gene symbol: FN1
  hgvsc: ENST00000357867.4:c.5591G>T
  hgvsp: ENSP00000350534.4:p.Gly1864Val
  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.5591G>T
  hgvsp: ENSP00000348285.4:p.Gly1864Val
  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.5861G>T
  hgvsp: ENSP00000265312.6:p.Gly1954Val
  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.5591G>T
  hgvsp: ENSP00000415018.1:p.Gly1864Val
  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.5861G>T
  hgvsp: ENSP00000349509.2:p.Gly1954Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.254G>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2012G>T
  hgvsp: ENSP00000416139.1:p.Gly671Val
  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.5861G>T
  hgvsp: ENSP00000410422.1:p.Gly1954Val
  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.6134G>T
  hgvsp: ENSP00000323534.6:p.Gly2045Val
  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.6134G>T
  hgvsp: ENSP00000346839.4:p.Gly2045Val
  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.5861G>T
  hgvsp: ENSP00000273049.7:p.Gly1954Val
  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.5861G>T
  hgvsp: ENSP00000352696.1:p.Gly1954Val
  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.5591G>T
  hgvsp: ENSP00000394423.1:p.Gly1864Val
  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.5864G>T
  hgvsp: ENSP00000399538.2:p.Gly1955Val
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7271G>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.218G>T
  hgvsp: ENSP00000392565.1:p.Gly73Val
  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.5861G>T
  hgvsp: ENSP00000338200.4:p.Gly1954Val
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly2045Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

2-216239962-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239962
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239962
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000338200
  ensembl transcript: ENST00000336916
  gene symbol: FN1
  hgvsc: ENST00000336916.4:c.5859T>C
  hgvsp: ENST00000336916.4:c.5859T>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.6132T>C
  hgvsp: ENST00000354785.4:c.6132T>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.5859T>C
  hgvsp: ENST00000346544.3:c.5859T>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.5589T>C
  hgvsp: ENST00000356005.4:c.5589T>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.5859T>C
  hgvsp: ENST00000359671.1:c.5859T>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.5589T>C
  hgvsp: ENST00000357867.4:c.5589T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2010T>C
  hgvsp: ENST00000456923.1:c.2010T>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.5589T>C
  hgvsp: ENST00000443816.1:c.5589T>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.5862T>C
  hgvsp: ENST00000432072.2:c.5862T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.252T>C
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7269T>C
  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.5859T>C
  hgvsp: ENST00000345488.5:c.5859T>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.6132T>C
  hgvsp: ENST00000323926.6:c.6132T>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.5859T>C
  hgvsp: ENST00000446046.1:c.5859T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.216T>C
  hgvsp: ENST00000438981.1:c.216T>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.5859T>C
  hgvsp: ENST00000357009.2:c.5859T>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.5589T>C
  hgvsp: ENST00000421182.1:c.5589T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro2044Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

2-216239963-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239963
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239963
    reference: chr 2
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
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.5861C>T
  hgvsp: ENSP00000399538.2:p.Pro1954Leu
  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.5858C>T
  hgvsp: ENSP00000338200.4:p.Pro1953Leu
  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.5588C>T
  hgvsp: ENSP00000415018.1:p.Pro1863Leu
  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.5858C>T
  hgvsp: ENSP00000352696.1:p.Pro1953Leu
  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.6131C>T
  hgvsp: ENSP00000323534.6:p.Pro2044Leu
  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.5858C>T
  hgvsp: ENSP00000265312.6:p.Pro1953Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.215C>T
  hgvsp: ENSP00000392565.1:p.Pro72Leu
  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.5588C>T
  hgvsp: ENSP00000348285.4:p.Pro1863Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2009C>T
  hgvsp: ENSP00000416139.1:p.Pro670Leu
  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.5858C>T
  hgvsp: ENSP00000273049.7:p.Pro1953Leu
  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.5858C>T
  hgvsp: ENSP00000410422.1:p.Pro1953Leu
  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.5588C>T
  hgvsp: ENSP00000394423.1:p.Pro1863Leu
  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.5588C>T
  hgvsp: ENSP00000350534.4:p.Pro1863Leu
  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.5858C>T
  hgvsp: ENSP00000349509.2:p.Pro1953Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.251C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7268C>T
  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.6131C>T
  hgvsp: ENSP00000346839.4:p.Pro2044Leu
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro2044Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

2-216239966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239966
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239966
    reference: chr 2
allele count: 2
allele frequency: 1.647690761397901e-5
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000265312
  ensembl transcript: ENST00000346544
  gene symbol: FN1
  hgvsc: ENST00000346544.3:c.5855G>A
  hgvsp: ENSP00000265312.6:p.Arg1952His
  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.6128G>A
  hgvsp: ENSP00000323534.6:p.Arg2043His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2006G>A
  hgvsp: ENSP00000416139.1:p.Arg669His
  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.5585G>A
  hgvsp: ENSP00000394423.1:p.Arg1862His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.248G>A
  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.5585G>A
  hgvsp: ENSP00000348285.4:p.Arg1862His
  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.6128G>A
  hgvsp: ENSP00000346839.4:p.Arg2043His
  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.5855G>A
  hgvsp: ENSP00000273049.7:p.Arg1952His
  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.5855G>A
  hgvsp: ENSP00000349509.2:p.Arg1952His
  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.5585G>A
  hgvsp: ENSP00000415018.1:p.Arg1862His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.212G>A
  hgvsp: ENSP00000392565.1:p.Arg71His
  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.5855G>A
  hgvsp: ENSP00000410422.1:p.Arg1952His
  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.5858G>A
  hgvsp: ENSP00000399538.2:p.Arg1953His
  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.5855G>A
  hgvsp: ENSP00000338200.4:p.Arg1952His
  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.5855G>A
  hgvsp: ENSP00000352696.1:p.Arg1952His
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7265G>A
  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.5585G>A
  hgvsp: ENSP00000350534.4:p.Arg1862His
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg2043His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

2-216239967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239967
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239967
    reference: chr 2
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000349509
  ensembl transcript: ENST00000357009
  gene symbol: FN1
  hgvsc: ENST00000357009.2:c.5854C>T
  hgvsp: ENSP00000349509.2:p.Arg1952Cys
  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.5854C>T
  hgvsp: ENSP00000273049.7:p.Arg1952Cys
  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.6127C>T
  hgvsp: ENSP00000323534.6:p.Arg2043Cys
  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.5857C>T
  hgvsp: ENSP00000399538.2:p.Arg1953Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.211C>T
  hgvsp: ENSP00000392565.1:p.Arg71Cys
  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.5584C>T
  hgvsp: ENSP00000415018.1:p.Arg1862Cys
  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.5854C>T
  hgvsp: ENSP00000352696.1:p.Arg1952Cys
  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.5854C>T
  hgvsp: ENSP00000410422.1:p.Arg1952Cys
  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.5584C>T
  hgvsp: ENSP00000394423.1:p.Arg1862Cys
  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.5584C>T
  hgvsp: ENSP00000348285.4:p.Arg1862Cys
  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.6127C>T
  hgvsp: ENSP00000346839.4:p.Arg2043Cys
  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.5854C>T
  hgvsp: ENSP00000265312.6:p.Arg1952Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7264C>T
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2005C>T
  hgvsp: ENSP00000416139.1:p.Arg669Cys
  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.5854C>T
  hgvsp: ENSP00000338200.4:p.Arg1952Cys
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.247C>T
  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.5584C>T
  hgvsp: ENSP00000350534.4:p.Arg1862Cys
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg2043Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

2-216239972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239972
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239972
    reference: chr 2
allele count: 3
allele frequency: 2.471454698235381e-5
allele num: 121386
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.5849G>A
  hgvsp: ENSP00000273049.7:p.Arg1950Gln
  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.5849G>A
  hgvsp: ENSP00000338200.4:p.Arg1950Gln
  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.6122G>A
  hgvsp: ENSP00000323534.6:p.Arg2041Gln
  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.5849G>A
  hgvsp: ENSP00000352696.1:p.Arg1950Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.206G>A
  hgvsp: ENSP00000392565.1:p.Arg69Gln
  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.5579G>A
  hgvsp: ENSP00000415018.1:p.Arg1860Gln
  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.5849G>A
  hgvsp: ENSP00000349509.2:p.Arg1950Gln
  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.5579G>A
  hgvsp: ENSP00000348285.4:p.Arg1860Gln
  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.6122G>A
  hgvsp: ENSP00000346839.4:p.Arg2041Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.2000G>A
  hgvsp: ENSP00000416139.1:p.Arg667Gln
  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.5579G>A
  hgvsp: ENSP00000350534.4:p.Arg1860Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7259G>A
  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.5852G>A
  hgvsp: ENSP00000399538.2:p.Arg1951Gln
  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.5849G>A
  hgvsp: ENSP00000265312.6:p.Arg1950Gln
  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.5579G>A
  hgvsp: ENSP00000394423.1:p.Arg1860Gln
  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.5849G>A
  hgvsp: ENSP00000410422.1:p.Arg1950Gln
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.242G>A
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg2041Gln
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

2-216239973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239973
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239973
    reference: chr 2
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
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.5848C>T
  hgvsp: ENSP00000410422.1:p.Arg1950Trp
  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.6121C>T
  hgvsp: ENSP00000323534.6:p.Arg2041Trp
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.1999C>T
  hgvsp: ENSP00000416139.1:p.Arg667Trp
  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.5578C>T
  hgvsp: ENSP00000415018.1:p.Arg1860Trp
  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.6121C>T
  hgvsp: ENSP00000346839.4:p.Arg2041Trp
  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.5848C>T
  hgvsp: ENSP00000265312.6:p.Arg1950Trp
  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.5848C>T
  hgvsp: ENSP00000273049.7:p.Arg1950Trp
  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.5848C>T
  hgvsp: ENSP00000349509.2:p.Arg1950Trp
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.205C>T
  hgvsp: ENSP00000392565.1:p.Arg69Trp
  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.5578C>T
  hgvsp: ENSP00000350534.4:p.Arg1860Trp
  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.5578C>T
  hgvsp: ENSP00000348285.4:p.Arg1860Trp
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7258C>T
  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.5848C>T
  hgvsp: ENSP00000338200.4:p.Arg1950Trp
  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.5848C>T
  hgvsp: ENSP00000352696.1:p.Arg1950Trp
  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.5851C>T
  hgvsp: ENSP00000399538.2:p.Arg1951Trp
  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.5578C>T
  hgvsp: ENSP00000394423.1:p.Arg1860Trp
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.241C>T
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg2041Trp
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

2-216239975-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239975
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239975
    reference: chr 2
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000273049
  ensembl transcript: ENST00000345488
  gene symbol: FN1
  hgvsc: ENST00000345488.5:c.5846C>G
  hgvsp: ENSP00000273049.7:p.Pro1949Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7256C>G
  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.5846C>G
  hgvsp: ENSP00000338200.4:p.Pro1949Arg
  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.5576C>G
  hgvsp: ENSP00000394423.1:p.Pro1859Arg
  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.5846C>G
  hgvsp: ENSP00000352696.1:p.Pro1949Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.203C>G
  hgvsp: ENSP00000392565.1:p.Pro68Arg
  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.5576C>G
  hgvsp: ENSP00000415018.1:p.Pro1859Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.239C>G
  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.5849C>G
  hgvsp: ENSP00000399538.2:p.Pro1950Arg
  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.5576C>G
  hgvsp: ENSP00000348285.4:p.Pro1859Arg
  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.5846C>G
  hgvsp: ENSP00000265312.6:p.Pro1949Arg
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.1997C>G
  hgvsp: ENSP00000416139.1:p.Pro666Arg
  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.6119C>G
  hgvsp: ENSP00000346839.4:p.Pro2040Arg
  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.5846C>G
  hgvsp: ENSP00000349509.2:p.Pro1949Arg
  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.5846C>G
  hgvsp: ENSP00000410422.1:p.Pro1949Arg
  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.5576C>G
  hgvsp: ENSP00000350534.4:p.Pro1859Arg
  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.6119C>G
  hgvsp: ENSP00000323534.6:p.Pro2040Arg
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro2040Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/2-216239982-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 216239982
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 216239982
    reference: chr 2
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000416139
  ensembl transcript: ENST00000456923
  gene symbol: FN1
  hgvsc: ENST00000456923.1:c.1990G>T
  hgvsp: ENSP00000416139.1:p.Val664Leu
  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.5842G>T
  hgvsp: ENSP00000399538.2:p.Val1948Leu
  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.5569G>T
  hgvsp: ENSP00000348285.4:p.Val1857Leu
  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.5839G>T
  hgvsp: ENSP00000273049.7:p.Val1947Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000460217
  gene symbol: FN1
  hgvsc: ENST00000460217.1:n.232G>T
  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.5839G>T
  hgvsp: ENSP00000352696.1:p.Val1947Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000115414
  ensembl protein: ENSP00000392565
  ensembl transcript: ENST00000438981
  gene symbol: FN1
  hgvsc: ENST00000438981.1:c.196G>T
  hgvsp: ENSP00000392565.1:p.Val66Leu
  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.6112G>T
  hgvsp: ENSP00000323534.6:p.Val2038Leu
  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.6112G>T
  hgvsp: ENSP00000346839.4:p.Val2038Leu
  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.5569G>T
  hgvsp: ENSP00000350534.4:p.Val1857Leu
  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.5839G>T
  hgvsp: ENSP00000338200.4:p.Val1947Leu
  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.5569G>T
  hgvsp: ENSP00000394423.1:p.Val1857Leu
  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.5569G>T
  hgvsp: ENSP00000415018.1:p.Val1857Leu
  variant of: http://identifiers.org/hgnc/3778
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000115414
  ensembl transcript: ENST00000492816
  gene symbol: FN1
  hgvsc: ENST00000492816.2:n.7249G>T
  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.5839G>T
  hgvsp: ENSP00000265312.6:p.Val1947Leu
  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.5839G>T
  hgvsp: ENSP00000410422.1:p.Val1947Leu
  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.5839G>T
  hgvsp: ENSP00000349509.2:p.Val1947Leu
  variant of: http://identifiers.org/hgnc/3778
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val2038Leu
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 1947
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 502
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 378
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5313
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1003
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11642
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 135
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 725
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1228
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 18405
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1454
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12765
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 183
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9605
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26759
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3128
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9182
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.056e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.940622e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.137e0

GenotypeDepth
all individuals: 724
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2924
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1945
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 501
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12609
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18298
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 584
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11610
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1189
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1228
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 313
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1000
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9168
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1811
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9600
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3829
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.958096729978461e-4
allele num: 10214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65930
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

QD
type: SiteQuality
SIO_000300: 1.786e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.41e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

DP
type: SiteQuality
SIO_000300: 1.936769e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

FS
type: SiteQuality
SIO_000300: 1.237e0

GenotypeDepth
all individuals: 2914
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9659
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16591
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 722
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10926
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5206
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1453
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 999
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4026
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 523
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 313
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1226
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1958
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21705
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1782
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2933
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8244
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9566
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1237
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.844457570387872e-5
allele num: 10158
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.085e1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 1.882119e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 3077
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 10771
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 538
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 998
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1227
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9489
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4549
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2920
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16343
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1450
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 722
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8181
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9567
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1190
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3658
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1738
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2715
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2224
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1233
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21130
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2905
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.87595e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.211e0

QD
type: SiteQuality
SIO_000300: 1.032e1

GenotypeDepth
all individuals: 1227
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 588
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10427
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2902
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5151
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 722
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3101
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 500
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 313
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9195
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 998
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1450
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5966
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2302
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2864
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7900
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9566
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 914
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2293
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3641
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19487
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523647001462701e-5
allele num: 65632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

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

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

MQ
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SIO_000300: 5.696e1

MQRankSum
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VQSLOD
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SIO_000300: -3.435e-1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 7.1e-3

FS
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SIO_000300: 1.3864e1

DP
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SIO_000300: 3.26556e6

QD
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SIO_000300: 1.111e1

ClippingRankSum
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SIO_000300: 1.14e0

BaseQRankSum
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SIO_000300: 4.32e0

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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

Other
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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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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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.23e-1

VQSLOD
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QD
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SIO_000300: 1.462e1

ClippingRankSum
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SIO_000300: 6.54e-1

InbreedingCoeff
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SIO_000300: 5.7e-3

MQRankSum
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SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 5.54e0

FS
type: SiteQuality
SIO_000300: 3.707e0

DP
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SIO_000300: 3.265745e6

GenotypeDepth
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variant carriers: 1

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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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.707e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.23e-1

DP
type: SiteQuality
SIO_000300: 3.265745e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.54e-1

QD
type: SiteQuality
SIO_000300: 1.462e1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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variant carriers: 29

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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variant carriers: 50

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 48
allele frequency: 4.61361014994233e-3
allele num: 10404
num of homozygotes: 0

Other
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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
allele num: 6614
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.267308e6

MQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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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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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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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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QD
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
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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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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

Other
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num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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FS
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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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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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Latino
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European (Non-Finnish)
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ClippingRankSum
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FS
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InbreedingCoeff
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DP
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QD
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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Latino
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European (Non-Finnish)
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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MQ
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InbreedingCoeff
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GenotypeQuality
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East Asian
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Latino
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allele frequency: 4.319281271596407e-4
allele num: 11576
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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VQSLOD
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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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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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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allele frequency: 0.0e0
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European (Non-Finnish)
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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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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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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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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

Latino
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Other
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African
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele num: 66722
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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QD
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
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SIO_000300: -4.4e-3

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

Latino
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Other
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African
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East Asian
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South Asian
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European (Non-Finnish)
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allele num: 66714
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MQ
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FS
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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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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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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num of homozygotes: 0

European (Finnish)
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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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Other
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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Latino
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East Asian
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African
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DP
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MQRankSum
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FS
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ClippingRankSum
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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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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European (Non-Finnish)
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African
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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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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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 (Non-Finnish)
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South Asian
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Other
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Latino
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European (Finnish)
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African
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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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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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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European (Finnish)
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East Asian
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South Asian
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African
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Other
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InbreedingCoeff
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DP
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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VQSLOD
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MQ
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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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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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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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Latino
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South Asian
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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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MQRankSum
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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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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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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East Asian
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European (Non-Finnish)
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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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Other
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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FS
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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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East Asian
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South Asian
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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MQ
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MQRankSum
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FS
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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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South Asian
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African
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Latino
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European (Finnish)
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Other
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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FS
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DP
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ReadPosRankSum
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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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East Asian
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South Asian
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African
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QD
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FS
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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QD
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FS
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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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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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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East Asian
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QD
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MQ
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VQSLOD
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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MQ
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FS
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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FS
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QD
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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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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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Latino
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South Asian
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East Asian
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African
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European (Finnish)
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Other
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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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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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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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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European (Finnish)
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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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South Asian
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FS
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BaseQRankSum
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VQSLOD
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DP
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QD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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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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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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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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African
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South Asian
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Other
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East Asian
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Latino
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European (Finnish)
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Latino
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Other
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European (Finnish)
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BaseQRankSum
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FS
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MQ
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DP
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VQSLOD
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GenotypeQuality
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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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MQRankSum
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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SIO_000300: -2.55e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.636e0

DP
type: SiteQuality
SIO_000300: 2.191742e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.079e1

GenotypeDepth
all individuals: 3483
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2129
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7667
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1558
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 315
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5351
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13457
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 638
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1177
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 852
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40481
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6634
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8784
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.349e1

FS
type: SiteQuality
SIO_000300: 5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

DP
type: SiteQuality
SIO_000300: 2.191488e6

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1558
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 638
bin: 7.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 382
bin: 7.75e1
variant carriers: 0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5351
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 852
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3482
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17821
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6633
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8783
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
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: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 8.183e0

QD
type: SiteQuality
SIO_000300: 3.48e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.309e0

VQSLOD
type: SiteQuality
SIO_000300: -6.589e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 2.191464e6