http://identifiers.org/exac.variant/9-131254930-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131254930
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131254930
    reference: chr 9
allele count: 1
allele frequency: 8.365120792344242e-6
allele num: 119544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1648-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1405-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1780-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1633-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1576-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1576-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1591-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1648-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1648-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1633-50A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1591-50A>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18594
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4652
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

9-131254937-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131254937
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131254937
    reference: chr 9
allele count: 14
allele frequency: 1.172568595262823e-4
allele num: 119396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1576-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1780-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1648-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1576-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1633-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1591-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1405-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1648-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1591-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1648-43C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1633-43C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19161
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4882
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19722
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6519
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2770
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-131254938-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131254938
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131254938
    reference: chr 9
allele count: 6
allele frequency: 5.017897166560734e-5
allele num: 119572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1576-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1591-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1648-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1648-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1648-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1633-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1405-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1576-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1780-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1591-42G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1633-42G>A
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4865
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20817
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 960
  bin: 5.25e1
  variant carriers: 0
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: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

9-131254942-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131254942
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131254942
    reference: chr 9
allele count: 1
allele frequency: 8.350591221858508e-6
allele num: 119752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1648-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1591-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1633-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1405-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1648-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1576-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1633-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1780-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1576-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1591-38C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1648-38C>G
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22397
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

9-131254954-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131254954
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131254954
    reference: chr 9
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1576-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1648-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1591-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1405-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1780-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1633-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1591-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1648-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1576-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1633-26T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1648-26T>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

9-131254966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131254966
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131254966
    reference: chr 9
allele count: 3
allele frequency: 2.484348603796085e-5
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1576-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1591-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1576-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1648-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1648-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1633-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1591-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1633-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1405-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1648-14T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1780-14T>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26617
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5613
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

9-131254968-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131254968
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131254968
    reference: chr 9
allele count: 1
allele frequency: 8.277597510098669e-6
allele num: 120808
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1648-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1648-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1576-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1780-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1591-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1633-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1405-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1633-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1576-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1591-12G>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1648-12G>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

9-131255016-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255016
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255016
    reference: chr 9
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1627G>T
  hgvsp: ENSP00000437579.1:p.Ala543Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1816G>T
  hgvsp: ENSP00000361901.3:p.Ala606Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1627G>T
  hgvsp: ENSP00000361877.3:p.Ala543Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1612G>T
  hgvsp: ENSP00000394506.2:p.Ala538Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1684G>T
  hgvsp: ENSP00000403453.2:p.Ala562Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1441G>T
  hgvsp: ENSP00000396687.2:p.Ala481Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1612G>T
  hgvsp: ENSP00000377161.5:p.Ala538Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1684G>T
  hgvsp: ENSP00000473949.2:p.Ala562Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1669G>T
  hgvsp: ENSP00000342581.3:p.Ala557Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1684G>T
  hgvsp: ENSP00000377166.2:p.Ala562Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1669G>T
  hgvsp: ENSP00000361893.5:p.Ala557Ser
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala562Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

9-131255020-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255020
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255020
    reference: chr 9
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1445A>G
  hgvsp: ENSP00000396687.2:p.Gln482Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1616A>G
  hgvsp: ENSP00000377161.5:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1820A>G
  hgvsp: ENSP00000361901.3:p.Gln607Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1688A>G
  hgvsp: ENSP00000473949.2:p.Gln563Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1688A>G
  hgvsp: ENSP00000377166.2:p.Gln563Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1673A>G
  hgvsp: ENSP00000361893.5:p.Gln558Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1616A>G
  hgvsp: ENSP00000394506.2:p.Gln539Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1631A>G
  hgvsp: ENSP00000437579.1:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1688A>G
  hgvsp: ENSP00000403453.2:p.Gln563Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1673A>G
  hgvsp: ENSP00000342581.3:p.Gln558Arg
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1631A>G
  hgvsp: ENSP00000361877.3:p.Gln544Arg
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5331
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln563Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

9-131255024-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255024
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255024
    reference: chr 9
allele count: 2
allele frequency: 1.65000165000165e-5
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1677A>G
  hgvsp: ENST00000372807.5:c.1677A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1449A>G
  hgvsp: ENST00000448249.3:c.1449A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1692A>G
  hgvsp: ENST00000604420.1:c.1692A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1677A>G
  hgvsp: ENST00000351030.3:c.1677A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1692A>G
  hgvsp: ENST00000393533.2:c.1692A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1620A>G
  hgvsp: ENST00000444119.2:c.1620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1635A>G
  hgvsp: ENST00000372791.3:c.1635A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1692A>G
  hgvsp: ENST00000434106.3:c.1692A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1620A>G
  hgvsp: ENST00000393527.3:c.1620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1824A>G
  hgvsp: ENST00000372814.3:c.1824A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1635A>G
  hgvsp: ENST00000546203.1:c.1635A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23169
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu564Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

9-131255028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255028
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255028
    reference: chr 9
allele count: 3
allele frequency: 2.475165836111019e-5
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1828C>T
  hgvsp: ENSP00000361901.3:p.Arg610Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1696C>T
  hgvsp: ENSP00000403453.2:p.Arg566Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1624C>T
  hgvsp: ENSP00000394506.2:p.Arg542Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1624C>T
  hgvsp: ENSP00000377161.5:p.Arg542Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1696C>T
  hgvsp: ENSP00000473949.2:p.Arg566Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1453C>T
  hgvsp: ENSP00000396687.2:p.Arg485Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1639C>T
  hgvsp: ENSP00000437579.1:p.Arg547Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1681C>T
  hgvsp: ENSP00000361893.5:p.Arg561Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1696C>T
  hgvsp: ENSP00000377166.2:p.Arg566Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1639C>T
  hgvsp: ENSP00000361877.3:p.Arg547Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1681C>T
  hgvsp: ENSP00000342581.3:p.Arg561Cys
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg566Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-131255065-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255065
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255065
    reference: chr 9
allele count: 3
allele frequency: 2.490494612229989e-5
allele num: 120458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1661T>C
  hgvsp: ENSP00000394506.2:p.Met554Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1718T>C
  hgvsp: ENSP00000361893.5:p.Met573Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1733T>C
  hgvsp: ENSP00000473949.2:p.Met578Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1676T>C
  hgvsp: ENSP00000361877.3:p.Met559Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1676T>C
  hgvsp: ENSP00000437579.1:p.Met559Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1490T>C
  hgvsp: ENSP00000396687.2:p.Met497Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1733T>C
  hgvsp: ENSP00000403453.2:p.Met578Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1733T>C
  hgvsp: ENSP00000377166.2:p.Met578Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1661T>C
  hgvsp: ENSP00000377161.5:p.Met554Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1718T>C
  hgvsp: ENSP00000342581.3:p.Met573Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1865T>C
  hgvsp: ENSP00000361901.3:p.Met622Thr
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23098
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met578Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

9-131255083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255083
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255083
    reference: chr 9
allele count: 1
allele frequency: 8.514986376021799e-6
allele num: 117440
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1679C>T
  hgvsp: ENSP00000394506.2:p.Ala560Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1883C>T
  hgvsp: ENSP00000361901.3:p.Ala628Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1736C>T
  hgvsp: ENSP00000342581.3:p.Ala579Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.11C>T
  hgvsp: ENSP00000474651.1:p.Ala4Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1751C>T
  hgvsp: ENSP00000473949.2:p.Ala584Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1751C>T
  hgvsp: ENSP00000377166.2:p.Ala584Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1736C>T
  hgvsp: ENSP00000361893.5:p.Ala579Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1679C>T
  hgvsp: ENSP00000377161.5:p.Ala560Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1694C>T
  hgvsp: ENSP00000437579.1:p.Ala565Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1508C>T
  hgvsp: ENSP00000396687.2:p.Ala503Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1694C>T
  hgvsp: ENSP00000361877.3:p.Ala565Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1751C>T
  hgvsp: ENSP00000403453.2:p.Ala584Val
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala584Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

9-131255084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255084
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255084
    reference: chr 9
allele count: 1
allele frequency: 8.542189875796559e-6
allele num: 117066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752G>A
  hgvsp: ENST00000604420.1:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752G>A
  hgvsp: ENST00000434106.3:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737G>A
  hgvsp: ENST00000351030.3:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752G>A
  hgvsp: ENST00000393533.2:c.1752G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737G>A
  hgvsp: ENST00000372807.5:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509G>A
  hgvsp: ENST00000448249.3:c.1509G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695G>A
  hgvsp: ENST00000546203.1:c.1695G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12G>A
  hgvsp: ENST00000483070.2:c.12G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680G>A
  hgvsp: ENST00000444119.2:c.1680G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695G>A
  hgvsp: ENST00000372791.3:c.1695G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884G>A
  hgvsp: ENST00000372814.3:c.1884G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680G>A
  hgvsp: ENST00000393527.3:c.1680G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1752G>A
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

9-131255092-TTTCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255092
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255088
    reference: chr 9
allele count: 1
allele frequency: 8.779168788299123e-6
allele num: 113906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+15_12+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+15_1884+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+15_1680+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+15_1695+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+15_1752+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+15_1695+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+15_1737+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+15_1752+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+15_1509+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+15_1737+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+15_1752+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+15_1680+18delCCTT
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: TTTCC
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

9-131255093-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255093
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255093
    reference: chr 9
allele count: 1
allele frequency: 8.781173164734809e-6
allele num: 113880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+9T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+9T>A
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19928
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

9-131255100-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255100
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255100
    reference: chr 9
allele count: 1
allele frequency: 9.012419113538457e-6
allele num: 110958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+16C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+16C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

9-131255109-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255109
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255109
    reference: chr 9
allele count: 7
allele frequency: 6.427679424079923e-5
allele num: 108904
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+25T>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12485
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17970
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

9-131255113-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255113
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255113
    reference: chr 9
allele count: 9
allele frequency: 8.354063787918168e-5
allele num: 107732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+29C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+29C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10535
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19511
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8313
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

9-131255125-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255125
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255125
    reference: chr 9
allele count: 2
allele frequency: 1.941898399875718e-5
allele num: 102992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+41C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+41C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19764
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-131255126-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255126
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255126
    reference: chr 9
allele count: 1
allele frequency: 9.724788485850432e-6
allele num: 102830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+42A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+42A>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

9-131255127-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255127
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255127
    reference: chr 9
allele count: 1
allele frequency: 9.786842568850437e-6
allele num: 102178
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+43T>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+43T>A
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19480
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

9-131255134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131255134
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131255134
    reference: chr 9
allele count: 1
allele frequency: 1.017749552190197e-5
allele num: 98256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1737+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1752+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.12+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1752+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1680+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1695+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1509+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1680+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1884+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1695+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1737+50C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1752+50C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18447
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

9-131256741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256741
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256741
    reference: chr 9
allele count: 187
allele frequency: 1.583269833206333e-3
allele num: 118110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-48C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 3.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 9470
  bin: 1.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19572
  bin: 2.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18559
  bin: 2.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/9-131256744-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256744
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256744
    reference: chr 9
allele count: 1
allele frequency: 8.460952703274388e-6
allele num: 118190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-45A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-45A>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

9-131256744-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256744
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256744
    reference: chr 9
allele count: 1
allele frequency: 8.460952703274388e-6
allele num: 118190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-45A>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-45A>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/9-131256745-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256745
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256745
    reference: chr 9
allele count: 1
allele frequency: 8.45594452900389e-6
allele num: 118260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-44A>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-44A>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

9-131256745-ACTGTGGGTCTTTCCTTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256745
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256728
    reference: chr 9
allele count: 266
allele frequency: 2.249281244715035e-3
allele num: 118260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 1.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18981
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22994
  bin: 2.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 3.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 2
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: ACTGTGGGTCTTTCCTTC
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

9-131256747-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256747
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256747
    reference: chr 9
allele count: 1
allele frequency: 8.4870911343846e-6
allele num: 117826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-42T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-42T>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24268
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19184
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-131256748-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256748
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256748
    reference: chr 9
allele count: 3
allele frequency: 2.545911266505991e-5
allele num: 117836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-41G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-41G>A
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24902
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS

9-131256754-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256754
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256754
    reference: chr 9
allele count: 1
allele frequency: 8.462957634434082e-6
allele num: 118162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-35C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-35C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20184
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

9-131256760-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256760
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256760
    reference: chr 9
allele count: 1
allele frequency: 8.430708010858751e-6
allele num: 118614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-29T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-29T>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20817
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

9-131256764-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256764
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256764
    reference: chr 9
allele count: 1
allele frequency: 8.366800535475235e-6
allele num: 119520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-25T>C
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-25T>C
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

9-131256769-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256769
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256769
    reference: chr 9
allele count: 272
allele frequency: 2.273791212465726e-3
allele num: 119624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-20G>A
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29589
  bin: 2.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 3.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21738
  bin: 2.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 33
genotype quality: GenotypeQuality
num of homozygotes: 4
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

9-131256779-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256779
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256779
    reference: chr 9
allele count: 3
allele frequency: 2.489006886252385e-5
allele num: 120530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696-10C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696-10C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

9-131256789-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256789
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256789
    reference: chr 9
allele count: 1
allele frequency: 8.268562923763849e-6
allele num: 120940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1696G>A
  hgvsp: ENSP00000437579.1:p.Ala566Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1738G>A
  hgvsp: ENSP00000361893.5:p.Ala580Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1681G>A
  hgvsp: ENSP00000377161.5:p.Ala561Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1738G>A
  hgvsp: ENSP00000342581.3:p.Ala580Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1753G>A
  hgvsp: ENSP00000473949.2:p.Ala585Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1753G>A
  hgvsp: ENSP00000403453.2:p.Ala585Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1681G>A
  hgvsp: ENSP00000394506.2:p.Ala561Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1510G>A
  hgvsp: ENSP00000396687.2:p.Ala504Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.13G>A
  hgvsp: ENSP00000474651.1:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1696G>A
  hgvsp: ENSP00000361877.3:p.Ala566Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1753G>A
  hgvsp: ENSP00000377166.2:p.Ala585Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1885G>A
  hgvsp: ENSP00000361901.3:p.Ala629Thr
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala585Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-131256790-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256790
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256790
    reference: chr 9
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1754C>A
  hgvsp: ENSP00000377166.2:p.Ala585Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1739C>A
  hgvsp: ENSP00000342581.3:p.Ala580Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1511C>A
  hgvsp: ENSP00000396687.2:p.Ala504Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.14C>A
  hgvsp: ENSP00000474651.1:p.Ala5Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1697C>A
  hgvsp: ENSP00000361877.3:p.Ala566Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1886C>A
  hgvsp: ENSP00000361901.3:p.Ala629Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1682C>A
  hgvsp: ENSP00000394506.2:p.Ala561Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1682C>A
  hgvsp: ENSP00000377161.5:p.Ala561Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1739C>A
  hgvsp: ENSP00000361893.5:p.Ala580Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1754C>A
  hgvsp: ENSP00000403453.2:p.Ala585Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1697C>A
  hgvsp: ENSP00000437579.1:p.Ala566Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1754C>A
  hgvsp: ENSP00000473949.2:p.Ala585Glu
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala585Glu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ

9-131256797-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256797
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256797
    reference: chr 9
allele count: 3
allele frequency: 2.475778632379884e-5
allele num: 121174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1761G>C
  hgvsp: ENSP00000473949.2:p.Arg587Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.21G>C
  hgvsp: ENSP00000474651.1:p.Arg7Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1704G>C
  hgvsp: ENSP00000361877.3:p.Arg568Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1761G>C
  hgvsp: ENSP00000377166.2:p.Arg587Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1704G>C
  hgvsp: ENSP00000437579.1:p.Arg568Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1746G>C
  hgvsp: ENSP00000342581.3:p.Arg582Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1746G>C
  hgvsp: ENSP00000361893.5:p.Arg582Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1893G>C
  hgvsp: ENSP00000361901.3:p.Arg631Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1689G>C
  hgvsp: ENSP00000377161.5:p.Arg563Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1689G>C
  hgvsp: ENSP00000394506.2:p.Arg563Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1518G>C
  hgvsp: ENSP00000396687.2:p.Arg506Ser
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1761G>C
  hgvsp: ENSP00000403453.2:p.Arg587Ser
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg587Ser
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

9-131256798-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256798
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256798
    reference: chr 9
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1690C>G
  hgvsp: ENSP00000394506.2:p.Gln564Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1762C>G
  hgvsp: ENSP00000377166.2:p.Gln588Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1894C>G
  hgvsp: ENSP00000361901.3:p.Gln632Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1762C>G
  hgvsp: ENSP00000473949.2:p.Gln588Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1690C>G
  hgvsp: ENSP00000377161.5:p.Gln564Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1747C>G
  hgvsp: ENSP00000361893.5:p.Gln583Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.22C>G
  hgvsp: ENSP00000474651.1:p.Gln8Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1705C>G
  hgvsp: ENSP00000361877.3:p.Gln569Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1747C>G
  hgvsp: ENSP00000342581.3:p.Gln583Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1519C>G
  hgvsp: ENSP00000396687.2:p.Gln507Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1705C>G
  hgvsp: ENSP00000437579.1:p.Gln569Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1762C>G
  hgvsp: ENSP00000403453.2:p.Gln588Glu
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5860
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln588Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

9-131256804-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256804
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256804
    reference: chr 9
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1525C>T
  hgvsp: ENSP00000396687.2:p.Gln509Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1696C>T
  hgvsp: ENSP00000377161.5:p.Gln566Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1696C>T
  hgvsp: ENSP00000394506.2:p.Gln566Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1768C>T
  hgvsp: ENSP00000473949.2:p.Gln590Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1768C>T
  hgvsp: ENSP00000377166.2:p.Gln590Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1711C>T
  hgvsp: ENSP00000361877.3:p.Gln571Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1753C>T
  hgvsp: ENSP00000361893.5:p.Gln585Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.28C>T
  hgvsp: ENSP00000474651.1:p.Gln10Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1900C>T
  hgvsp: ENSP00000361901.3:p.Gln634Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1768C>T
  hgvsp: ENSP00000403453.2:p.Gln590Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1711C>T
  hgvsp: ENSP00000437579.1:p.Gln571Ter
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1753C>T
  hgvsp: ENSP00000342581.3:p.Gln585Ter
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln590Ter
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

9-131256817-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256817
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256817
    reference: chr 9
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1538C>G
  hgvsp: ENSP00000396687.2:p.Ala513Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1709C>G
  hgvsp: ENSP00000377161.5:p.Ala570Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1781C>G
  hgvsp: ENSP00000377166.2:p.Ala594Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1781C>G
  hgvsp: ENSP00000473949.2:p.Ala594Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1766C>G
  hgvsp: ENSP00000361893.5:p.Ala589Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1781C>G
  hgvsp: ENSP00000403453.2:p.Ala594Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.41C>G
  hgvsp: ENSP00000474651.1:p.Ala14Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1709C>G
  hgvsp: ENSP00000394506.2:p.Ala570Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1913C>G
  hgvsp: ENSP00000361901.3:p.Ala638Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1766C>G
  hgvsp: ENSP00000342581.3:p.Ala589Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1724C>G
  hgvsp: ENSP00000361877.3:p.Ala575Gly
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1724C>G
  hgvsp: ENSP00000437579.1:p.Ala575Gly
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala594Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

9-131256824-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256824
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256824
    reference: chr 9
allele count: 5
allele frequency: 4.121535849118816e-5
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1773G>T
  hgvsp: ENST00000351030.3:c.1773G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1788G>T
  hgvsp: ENST00000393533.2:c.1788G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1731G>T
  hgvsp: ENST00000546203.1:c.1731G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1920G>T
  hgvsp: ENST00000372814.3:c.1920G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1731G>T
  hgvsp: ENST00000372791.3:c.1731G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1788G>T
  hgvsp: ENST00000604420.1:c.1788G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1716G>T
  hgvsp: ENST00000393527.3:c.1716G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1716G>T
  hgvsp: ENST00000444119.2:c.1716G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1545G>T
  hgvsp: ENST00000448249.3:c.1545G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.48G>T
  hgvsp: ENST00000483070.2:c.48G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1773G>T
  hgvsp: ENST00000372807.5:c.1773G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1788G>T
  hgvsp: ENST00000434106.3:c.1788G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu596Leu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

9-131256827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256827
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256827
    reference: chr 9
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1719G>A
  hgvsp: ENST00000444119.2:c.1719G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1791G>A
  hgvsp: ENST00000604420.1:c.1791G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1719G>A
  hgvsp: ENST00000393527.3:c.1719G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1548G>A
  hgvsp: ENST00000448249.3:c.1548G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.51G>A
  hgvsp: ENST00000483070.2:c.51G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1734G>A
  hgvsp: ENST00000372791.3:c.1734G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1791G>A
  hgvsp: ENST00000393533.2:c.1791G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1776G>A
  hgvsp: ENST00000351030.3:c.1776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1776G>A
  hgvsp: ENST00000372807.5:c.1776G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1791G>A
  hgvsp: ENST00000434106.3:c.1791G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1734G>A
  hgvsp: ENST00000546203.1:c.1734G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1923G>A
  hgvsp: ENST00000372814.3:c.1923G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln597Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

9-131256833-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256833
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256833
    reference: chr 9
allele count: 19
allele frequency: 1.566209443418623e-4
allele num: 121312
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1797C>G
  hgvsp: ENST00000434106.3:c.1797C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1797C>G
  hgvsp: ENST00000604420.1:c.1797C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1929C>G
  hgvsp: ENST00000372814.3:c.1929C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1782C>G
  hgvsp: ENST00000351030.3:c.1782C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1725C>G
  hgvsp: ENST00000444119.2:c.1725C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1740C>G
  hgvsp: ENST00000372791.3:c.1740C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1782C>G
  hgvsp: ENST00000372807.5:c.1782C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1554C>G
  hgvsp: ENST00000448249.3:c.1554C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.57C>G
  hgvsp: ENST00000483070.2:c.57C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1797C>G
  hgvsp: ENST00000393533.2:c.1797C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1740C>G
  hgvsp: ENST00000546203.1:c.1740C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1725C>G
  hgvsp: ENST00000393527.3:c.1725C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23531
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu599Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

9-131256853-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256853
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256853
    reference: chr 9
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1760C>T
  hgvsp: ENSP00000361877.3:p.Thr587Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1817C>T
  hgvsp: ENSP00000473949.2:p.Thr606Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1745C>T
  hgvsp: ENSP00000377161.5:p.Thr582Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1802C>T
  hgvsp: ENSP00000342581.3:p.Thr601Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1949C>T
  hgvsp: ENSP00000361901.3:p.Thr650Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1574C>T
  hgvsp: ENSP00000396687.2:p.Thr525Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1745C>T
  hgvsp: ENSP00000394506.2:p.Thr582Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1760C>T
  hgvsp: ENSP00000437579.1:p.Thr587Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1817C>T
  hgvsp: ENSP00000377166.2:p.Thr606Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1802C>T
  hgvsp: ENSP00000361893.5:p.Thr601Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1817C>T
  hgvsp: ENSP00000403453.2:p.Thr606Met
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.77C>T
  hgvsp: ENSP00000474651.1:p.Thr26Met
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr606Met
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

9-131256854-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256854
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256854
    reference: chr 9
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1818G>A
  hgvsp: ENST00000434106.3:c.1818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1818G>A
  hgvsp: ENST00000604420.1:c.1818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.78G>A
  hgvsp: ENST00000483070.2:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1803G>A
  hgvsp: ENST00000372807.5:c.1803G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1746G>A
  hgvsp: ENST00000393527.3:c.1746G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1950G>A
  hgvsp: ENST00000372814.3:c.1950G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1803G>A
  hgvsp: ENST00000351030.3:c.1803G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1575G>A
  hgvsp: ENST00000448249.3:c.1575G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1818G>A
  hgvsp: ENST00000393533.2:c.1818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1761G>A
  hgvsp: ENST00000372791.3:c.1761G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1746G>A
  hgvsp: ENST00000444119.2:c.1746G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1761G>A
  hgvsp: ENST00000546203.1:c.1761G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29638
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr606Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

9-131256867-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256867
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256867
    reference: chr 9
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1831G>A
  hgvsp: ENSP00000403453.2:p.Ala611Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1774G>A
  hgvsp: ENSP00000437579.1:p.Ala592Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.91G>A
  hgvsp: ENSP00000474651.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1831G>A
  hgvsp: ENSP00000377166.2:p.Ala611Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1816G>A
  hgvsp: ENSP00000361893.5:p.Ala606Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1963G>A
  hgvsp: ENSP00000361901.3:p.Ala655Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1759G>A
  hgvsp: ENSP00000377161.5:p.Ala587Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1831G>A
  hgvsp: ENSP00000473949.2:p.Ala611Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1588G>A
  hgvsp: ENSP00000396687.2:p.Ala530Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1759G>A
  hgvsp: ENSP00000394506.2:p.Ala587Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1816G>A
  hgvsp: ENSP00000342581.3:p.Ala606Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1774G>A
  hgvsp: ENSP00000361877.3:p.Ala592Thr
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala611Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

9-131256869-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256869
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256869
    reference: chr 9
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1761T>C
  hgvsp: ENST00000444119.2:c.1761T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1818T>C
  hgvsp: ENST00000351030.3:c.1818T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1776T>C
  hgvsp: ENST00000372791.3:c.1776T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1833T>C
  hgvsp: ENST00000604420.1:c.1833T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1776T>C
  hgvsp: ENST00000546203.1:c.1776T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1833T>C
  hgvsp: ENST00000434106.3:c.1833T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1590T>C
  hgvsp: ENST00000448249.3:c.1590T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.93T>C
  hgvsp: ENST00000483070.2:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1818T>C
  hgvsp: ENST00000372807.5:c.1818T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1761T>C
  hgvsp: ENST00000393527.3:c.1761T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1833T>C
  hgvsp: ENST00000393533.2:c.1833T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1965T>C
  hgvsp: ENST00000372814.3:c.1965T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala611Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

9-131256878-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256878
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256878
    reference: chr 9
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1842A>G
  hgvsp: ENST00000393533.2:c.1842A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1770A>G
  hgvsp: ENST00000393527.3:c.1770A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.102A>G
  hgvsp: ENST00000483070.2:c.102A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1599A>G
  hgvsp: ENST00000448249.3:c.1599A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1974A>G
  hgvsp: ENST00000372814.3:c.1974A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1785A>G
  hgvsp: ENST00000372791.3:c.1785A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1827A>G
  hgvsp: ENST00000372807.5:c.1827A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1770A>G
  hgvsp: ENST00000444119.2:c.1770A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1842A>G
  hgvsp: ENST00000604420.1:c.1842A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1842A>G
  hgvsp: ENST00000434106.3:c.1842A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1827A>G
  hgvsp: ENST00000351030.3:c.1827A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1785A>G
  hgvsp: ENST00000546203.1:c.1785A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln614Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD

9-131256884-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256884
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256884
    reference: chr 9
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1833A>G
  hgvsp: ENST00000372807.5:c.1833A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1848A>G
  hgvsp: ENST00000604420.1:c.1848A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1776A>G
  hgvsp: ENST00000393527.3:c.1776A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1833A>G
  hgvsp: ENST00000351030.3:c.1833A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1848A>G
  hgvsp: ENST00000393533.2:c.1848A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1605A>G
  hgvsp: ENST00000448249.3:c.1605A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1791A>G
  hgvsp: ENST00000546203.1:c.1791A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.108A>G
  hgvsp: ENST00000483070.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1791A>G
  hgvsp: ENST00000372791.3:c.1791A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1980A>G
  hgvsp: ENST00000372814.3:c.1980A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1776A>G
  hgvsp: ENST00000444119.2:c.1776A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1848A>G
  hgvsp: ENST00000434106.3:c.1848A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln616Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

9-131256894-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256894
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256894
    reference: chr 9
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.118T>C
  hgvsp: ENSP00000474651.1:p.Tyr40His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1801T>C
  hgvsp: ENSP00000437579.1:p.Tyr601His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1843T>C
  hgvsp: ENSP00000342581.3:p.Tyr615His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1615T>C
  hgvsp: ENSP00000396687.2:p.Tyr539His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1858T>C
  hgvsp: ENSP00000473949.2:p.Tyr620His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1858T>C
  hgvsp: ENSP00000377166.2:p.Tyr620His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.1990T>C
  hgvsp: ENSP00000361901.3:p.Tyr664His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1786T>C
  hgvsp: ENSP00000394506.2:p.Tyr596His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1801T>C
  hgvsp: ENSP00000361877.3:p.Tyr601His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1858T>C
  hgvsp: ENSP00000403453.2:p.Tyr620His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1786T>C
  hgvsp: ENSP00000377161.5:p.Tyr596His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1843T>C
  hgvsp: ENSP00000361893.5:p.Tyr615His
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr620His
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD

9-131256909-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256909
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256909
    reference: chr 9
allele count: 3
allele frequency: 2.473166147301776e-5
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1858A>G
  hgvsp: ENSP00000361893.5:p.Ile620Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1873A>G
  hgvsp: ENSP00000403453.2:p.Ile625Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1816A>G
  hgvsp: ENSP00000361877.3:p.Ile606Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1858A>G
  hgvsp: ENSP00000342581.3:p.Ile620Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1873A>G
  hgvsp: ENSP00000473949.2:p.Ile625Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1873A>G
  hgvsp: ENSP00000377166.2:p.Ile625Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2005A>G
  hgvsp: ENSP00000361901.3:p.Ile669Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1630A>G
  hgvsp: ENSP00000396687.2:p.Ile544Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1801A>G
  hgvsp: ENSP00000394506.2:p.Ile601Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1816A>G
  hgvsp: ENSP00000437579.1:p.Ile606Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1801A>G
  hgvsp: ENSP00000377161.5:p.Ile601Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.133A>G
  hgvsp: ENSP00000474651.1:p.Ile45Val
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ile625Val
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

9-131256911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256911
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256911
    reference: chr 9
allele count: 9
allele frequency: 7.419743112005144e-5
allele num: 121298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1818C>T
  hgvsp: ENST00000372791.3:c.1818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2007C>T
  hgvsp: ENST00000372814.3:c.2007C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1860C>T
  hgvsp: ENST00000351030.3:c.1860C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1875C>T
  hgvsp: ENST00000604420.1:c.1875C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1803C>T
  hgvsp: ENST00000444119.2:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.135C>T
  hgvsp: ENST00000483070.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1632C>T
  hgvsp: ENST00000448249.3:c.1632C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1818C>T
  hgvsp: ENST00000546203.1:c.1818C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1875C>T
  hgvsp: ENST00000434106.3:c.1875C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1875C>T
  hgvsp: ENST00000393533.2:c.1875C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1803C>T
  hgvsp: ENST00000393527.3:c.1803C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1860C>T
  hgvsp: ENST00000372807.5:c.1860C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile625Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

9-131256920-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256920
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256920
    reference: chr 9
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1812A>T
  hgvsp: ENST00000393527.3:c.1812A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1827A>T
  hgvsp: ENST00000372791.3:c.1827A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1827A>T
  hgvsp: ENST00000546203.1:c.1827A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.144A>T
  hgvsp: ENST00000483070.2:c.144A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1869A>T
  hgvsp: ENST00000351030.3:c.1869A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1641A>T
  hgvsp: ENST00000448249.3:c.1641A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1884A>T
  hgvsp: ENST00000393533.2:c.1884A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1884A>T
  hgvsp: ENST00000604420.1:c.1884A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1884A>T
  hgvsp: ENST00000434106.3:c.1884A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2016A>T
  hgvsp: ENST00000372814.3:c.2016A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1812A>T
  hgvsp: ENST00000444119.2:c.1812A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1869A>T
  hgvsp: ENST00000372807.5:c.1869A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5861
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr628Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

9-131256924-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256924
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256924
    reference: chr 9
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1831A>G
  hgvsp: ENSP00000361877.3:p.Ile611Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1816A>G
  hgvsp: ENSP00000394506.2:p.Ile606Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.148A>G
  hgvsp: ENSP00000474651.1:p.Ile50Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1873A>G
  hgvsp: ENSP00000342581.3:p.Ile625Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1888A>G
  hgvsp: ENSP00000377166.2:p.Ile630Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1888A>G
  hgvsp: ENSP00000473949.2:p.Ile630Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1831A>G
  hgvsp: ENSP00000437579.1:p.Ile611Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1873A>G
  hgvsp: ENSP00000361893.5:p.Ile625Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1645A>G
  hgvsp: ENSP00000396687.2:p.Ile549Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1816A>G
  hgvsp: ENSP00000377161.5:p.Ile606Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1888A>G
  hgvsp: ENSP00000403453.2:p.Ile630Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2020A>G
  hgvsp: ENSP00000361901.3:p.Ile674Val
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile630Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-131256925-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256925
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256925
    reference: chr 9
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1832T>C
  hgvsp: ENSP00000361877.3:p.Ile611Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1832T>C
  hgvsp: ENSP00000437579.1:p.Ile611Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1646T>C
  hgvsp: ENSP00000396687.2:p.Ile549Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1889T>C
  hgvsp: ENSP00000377166.2:p.Ile630Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.149T>C
  hgvsp: ENSP00000474651.1:p.Ile50Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1817T>C
  hgvsp: ENSP00000377161.5:p.Ile606Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1889T>C
  hgvsp: ENSP00000403453.2:p.Ile630Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1874T>C
  hgvsp: ENSP00000342581.3:p.Ile625Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1889T>C
  hgvsp: ENSP00000473949.2:p.Ile630Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1874T>C
  hgvsp: ENSP00000361893.5:p.Ile625Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2021T>C
  hgvsp: ENSP00000361901.3:p.Ile674Thr
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1817T>C
  hgvsp: ENSP00000394506.2:p.Ile606Thr
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile630Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

9-131256946-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256946
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256946
    reference: chr 9
allele count: 2
allele frequency: 1.652674026574998e-5
allele num: 121016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1895G>A
  hgvsp: ENSP00000342581.3:p.Arg632Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2042G>A
  hgvsp: ENSP00000361901.3:p.Arg681Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1838G>A
  hgvsp: ENSP00000377161.5:p.Arg613Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1910G>A
  hgvsp: ENSP00000403453.2:p.Arg637Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1838G>A
  hgvsp: ENSP00000394506.2:p.Arg613Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1667G>A
  hgvsp: ENSP00000396687.2:p.Arg556Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1910G>A
  hgvsp: ENSP00000377166.2:p.Arg637Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1895G>A
  hgvsp: ENSP00000361893.5:p.Arg632Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1853G>A
  hgvsp: ENSP00000361877.3:p.Arg618Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1910G>A
  hgvsp: ENSP00000473949.2:p.Arg637Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.170G>A
  hgvsp: ENSP00000474651.1:p.Arg57Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1853G>A
  hgvsp: ENSP00000437579.1:p.Arg618Gln
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg637Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

9-131256946-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256946
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256946
    reference: chr 9
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1895G>C
  hgvsp: ENSP00000361893.5:p.Arg632Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1910G>C
  hgvsp: ENSP00000473949.2:p.Arg637Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1838G>C
  hgvsp: ENSP00000394506.2:p.Arg613Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1910G>C
  hgvsp: ENSP00000377166.2:p.Arg637Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1667G>C
  hgvsp: ENSP00000396687.2:p.Arg556Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1910G>C
  hgvsp: ENSP00000403453.2:p.Arg637Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1853G>C
  hgvsp: ENSP00000361877.3:p.Arg618Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1838G>C
  hgvsp: ENSP00000377161.5:p.Arg613Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.170G>C
  hgvsp: ENSP00000474651.1:p.Arg57Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2042G>C
  hgvsp: ENSP00000361901.3:p.Arg681Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1853G>C
  hgvsp: ENSP00000437579.1:p.Arg618Pro
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1895G>C
  hgvsp: ENSP00000342581.3:p.Arg632Pro
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg637Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-131256948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256948
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256948
    reference: chr 9
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1669G>A
  hgvsp: ENSP00000396687.2:p.Val557Ile
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+1G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+1G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+1G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+1G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+1G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1855G>A
  hgvsp: ENSP00000437579.1:p.Val619Ile
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1855G>A
  hgvsp: ENSP00000361877.3:p.Val619Ile
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+1G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+1G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2044G>A
  hgvsp: ENSP00000361901.3:p.Val682Ile
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1912G>A
  hgvsp: ENSP00000377166.2:p.Val638Ile
  variant of: http://identifiers.org/hgnc/8114
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29483
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1911+1G>A
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

9-131256967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256967
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256967
    reference: chr 9
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1874G>A
  hgvsp: ENSP00000437579.1:p.Gly625Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2063G>A
  hgvsp: ENSP00000361901.3:p.Gly688Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1688G>A
  hgvsp: ENSP00000396687.2:p.Gly563Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1931G>A
  hgvsp: ENSP00000377166.2:p.Gly644Glu
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+20G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1874G>A
  hgvsp: ENSP00000361877.3:p.Gly625Glu
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly688Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum

9-131256970-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256970
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256970
    reference: chr 9
allele count: 2
allele frequency: 1.658072325114821e-5
allele num: 120622
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1877C>G
  hgvsp: ENSP00000361877.3:p.Ser626Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+23C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1877C>G
  hgvsp: ENSP00000437579.1:p.Ser626Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+23C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+23C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+23C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1691C>G
  hgvsp: ENSP00000396687.2:p.Ser564Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2066C>G
  hgvsp: ENSP00000361901.3:p.Ser689Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1934C>G
  hgvsp: ENSP00000377166.2:p.Ser645Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+23C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+23C>G
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+23C>G
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser689Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

9-131256974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256974
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256974
    reference: chr 9
allele count: 3
allele frequency: 2.491115023084333e-5
allele num: 120428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+27C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+27C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+27C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+27C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1695C>T
  hgvsp: ENST00000448249.3:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2070C>T
  hgvsp: ENST00000372814.3:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1881C>T
  hgvsp: ENST00000372791.3:c.1881C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+27C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+27C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+27C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1881C>T
  hgvsp: ENST00000546203.1:c.1881C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1938C>T
  hgvsp: ENST00000393533.2:c.1938C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His690His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

9-131256985-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256985
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256985
    reference: chr 9
allele count: 1
allele frequency: 8.330695279828055e-6
allele num: 120038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+38G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1949G>A
  hgvsp: ENSP00000377166.2:p.Arg650Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1892G>A
  hgvsp: ENSP00000437579.1:p.Arg631Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1892G>A
  hgvsp: ENSP00000361877.3:p.Arg631Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+38G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2081G>A
  hgvsp: ENSP00000361901.3:p.Arg694Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1706G>A
  hgvsp: ENSP00000396687.2:p.Arg569Gln
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+38G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+38G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+38G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+38G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+38G>A
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg694Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

9-131256994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256994
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256994
    reference: chr 9
allele count: 1
allele frequency: 8.37058242512514e-6
allele num: 119466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1715C>T
  hgvsp: ENSP00000396687.2:p.Ala572Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+47C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+47C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1901C>T
  hgvsp: ENSP00000361877.3:p.Ala634Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+47C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2090C>T
  hgvsp: ENSP00000361901.3:p.Ala697Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+47C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+47C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1901C>T
  hgvsp: ENSP00000437579.1:p.Ala634Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+47C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1958C>T
  hgvsp: ENSP00000377166.2:p.Ala653Val
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+47C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28463
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala697Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

9-131256995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256995
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256995
    reference: chr 9
allele count: 1
allele frequency: 8.375910880308233e-6
allele num: 119390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1959C>T
  hgvsp: ENST00000393533.2:c.1959C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2091C>T
  hgvsp: ENST00000372814.3:c.2091C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1716C>T
  hgvsp: ENST00000448249.3:c.1716C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1902C>T
  hgvsp: ENST00000546203.1:c.1902C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1902C>T
  hgvsp: ENST00000372791.3:c.1902C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+48C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+48C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala697Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

9-131256996-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256996
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256996
    reference: chr 9
allele count: 2
allele frequency: 1.676727028839705e-5
allele num: 119280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1960C>T
  hgvsp: ENSP00000377166.2:p.Arg654Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1903C>T
  hgvsp: ENSP00000361877.3:p.Arg635Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2092C>T
  hgvsp: ENSP00000361901.3:p.Arg698Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+49C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1717C>T
  hgvsp: ENSP00000396687.2:p.Arg573Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+49C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1903C>T
  hgvsp: ENSP00000437579.1:p.Arg635Cys
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+49C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+49C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+49C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+49C>T
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+49C>T
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5563
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg698Cys
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

9-131256997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131256997
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 131256997
    reference: chr 9
allele count: 3
allele frequency: 2.518384204694268e-5
allele num: 119124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000394506
  ensembl transcript: ENST00000444119
  gene symbol: ODF2
  hgvsc: ENST00000444119.2:c.1839+50G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377161
  ensembl transcript: ENST00000393527
  gene symbol: ODF2
  hgvsc: ENST00000393527.3:c.1839+50G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361877
  ensembl transcript: ENST00000372791
  gene symbol: ODF2
  hgvsc: ENST00000372791.3:c.1904G>A
  hgvsp: ENSP00000361877.3:p.Arg635His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000396687
  ensembl transcript: ENST00000448249
  gene symbol: ODF2
  hgvsc: ENST00000448249.3:c.1718G>A
  hgvsp: ENSP00000396687.2:p.Arg573His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361901
  ensembl transcript: ENST00000372814
  gene symbol: ODF2
  hgvsc: ENST00000372814.3:c.2093G>A
  hgvsp: ENSP00000361901.3:p.Arg698His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000342581
  ensembl transcript: ENST00000351030
  gene symbol: ODF2
  hgvsc: ENST00000351030.3:c.1896+50G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000403453
  ensembl transcript: ENST00000434106
  gene symbol: ODF2
  hgvsc: ENST00000434106.3:c.1911+50G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000473949
  ensembl transcript: ENST00000604420
  gene symbol: ODF2
  hgvsc: ENST00000604420.1:c.1911+50G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000361893
  ensembl transcript: ENST00000372807
  gene symbol: ODF2
  hgvsc: ENST00000372807.5:c.1896+50G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000437579
  ensembl transcript: ENST00000546203
  gene symbol: ODF2
  hgvsc: ENST00000546203.1:c.1904G>A
  hgvsp: ENSP00000437579.1:p.Arg635His
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000474651
  ensembl transcript: ENST00000483070
  gene symbol: ODF2
  hgvsc: ENST00000483070.2:c.171+50G>A
  variant of: http://identifiers.org/hgnc/8114
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000136811
  ensembl protein: ENSP00000377166
  ensembl transcript: ENST00000393533
  gene symbol: ODF2
  hgvsc: ENST00000393533.2:c.1961G>A
  hgvsp: ENSP00000377166.2:p.Arg654His
  variant of: http://identifiers.org/hgnc/8114
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28028
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg698His
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G

GenotypeQuality
all individuals: 1362
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27360
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5234
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1219
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4400
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3003
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1348
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16232
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65794
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.732e0

DP
type: SiteQuality
SIO_000300: 1.713235e6

MQRankSum
type: SiteQuality
SIO_000300: 2.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.669e-1

FS
type: SiteQuality
SIO_000300: 9.747999999999999e0

QD
type: SiteQuality
SIO_000300: 1.683e1

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1472
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5057
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2090
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33782
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1404
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4659
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 2717
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.179523472517103e-4
allele num: 8478
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.121076233183856e-3
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 8
allele frequency: 4.939491232403062e-4
allele num: 16196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.085501293169025e-5
allele num: 65730
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.776e0

DP
type: SiteQuality
SIO_000300: 1.735325e6

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.457e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

GenotypeQuality
all individuals: 1117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5165
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1380
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4651
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 493
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.117986748525926e-5
allele num: 65804
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11334
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
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SIO_000300: 4.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQ
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SIO_000300: 5.97e1

FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.74273e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

QD
type: SiteQuality
SIO_000300: 1.324e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65926
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.148548942449582e-5
allele num: 16264
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

InbreedingCoeff
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: -9.64e-1

VQSLOD
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MQRankSum
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SIO_000300: -3.9e-2

ClippingRankSum
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SIO_000300: 1.16e-1

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.432e1

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66188
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 8.771929824561403e-5
allele num: 11400
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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VQSLOD
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FS
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SIO_000300: 3.164e0

QD
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BaseQRankSum
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SIO_000300: 3.42e0

ClippingRankSum
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SIO_000300: -3.91e-1

MQRankSum
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SIO_000300: 1.27e0

MQ
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SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 1.800244e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 3.472222222222222e-4
allele num: 8640
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.543e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
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SIO_000300: 7.0e-4

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.496e1

MQ
type: SiteQuality
SIO_000300: 5.836e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

BaseQRankSum
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SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 8.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.691800736576855e-5
allele num: 10318
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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 1.39e-1

BaseQRankSum
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 2.93e-1

MQRankSum
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DP
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SIO_000300: 1.823744e6

ReadPosRankSum
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SIO_000300: -8.8e-1

QD
type: SiteQuality
SIO_000300: 1.513e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

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 frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

Other
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66662
num of homozygotes: 0

European (Finnish)
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South Asian
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East Asian
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Other
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BaseQRankSum
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ClippingRankSum
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QD
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DP
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VQSLOD
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ReadPosRankSum
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

South Asian
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allele num: 16486
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

South Asian
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allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000840235265874e-5
allele num: 66648
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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Other
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MQ
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SIO_000300: 5.974e1

VQSLOD
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FS
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DP
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
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Latino
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allele count: 2
allele frequency: 1.748863238894718e-4
allele num: 11436
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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: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 64460
num of homozygotes: 0

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

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

European (Finnish)
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 61218
num of homozygotes: 0

Latino
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South Asian
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East Asian
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Other
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MQRankSum
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MQ
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QD
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BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Other
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allele count: 1
allele frequency: 1.228501228501228e-3
allele num: 814
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60188
num of homozygotes: 0

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

African
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allele count: 5
allele frequency: 5.406574394463668e-4
allele num: 9248
num of homozygotes: 0

Latino
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allele frequency: 1.000200040008002e-4
allele num: 9998
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e-1

InbreedingCoeff
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SIO_000300: -1.6e-3

MQRankSum
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SIO_000300: 3.04e-1

BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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SIO_000300: 3.261e0

VQSLOD
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SIO_000300: 1.26e0

QD
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SIO_000300: 1.638e1

DP
type: SiteQuality
SIO_000300: 1.465768e6

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 9
allele frequency: 1.509307395606238e-4
allele num: 59630
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 14624
num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

BaseQRankSum
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DP
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FS
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SIO_000300: 6.5e-1

MQ
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InbreedingCoeff
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SIO_000300: -2.2e-3

MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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SIO_000300: -1.68e-1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5950
num of homozygotes: 0

Latino
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East Asian
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allele frequency: 0.0e0
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African
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South Asian
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Other
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European (Non-Finnish)
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allele frequency: 3.506065493303415e-5
allele num: 57044
num of homozygotes: 0

FS
type: SiteQuality
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InbreedingCoeff
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MQ
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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MQRankSum
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SIO_000300: 7.76e-1

BaseQRankSum
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GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.756481416426614e-5
allele num: 56932
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13972
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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East Asian
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BaseQRankSum
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SIO_000300: 4.47e0

MQRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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SIO_000300: 5.94e1

ClippingRankSum
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SIO_000300: -5.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.18e-1

DP
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GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9232
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.768346595932803e-5
allele num: 56550
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

South Asian
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VQSLOD
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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SIO_000300: 4.69e0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5774
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6776
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Other
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 1.147052076164258e-4
allele num: 8718
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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BaseQRankSum
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SIO_000300: -3.163e0

MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64758
num of homozygotes: 0

Other
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East Asian
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African
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allele count: 173
allele frequency: 1.70746150809317e-2
allele num: 10132
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele count: 11
allele frequency: 9.743135518157661e-4
allele num: 11290
num of homozygotes: 0

South Asian
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allele num: 16244
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MQRankSum
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SIO_000300: 2.11e-1

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

GenotypeQuality
all individuals: 35365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1414
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6003
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.875567845151097e-5
allele num: 10126
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.763e1

DP
type: SiteQuality
SIO_000300: 1.402739e6

FS
type: SiteQuality
SIO_000300: 1.549e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

QD
type: SiteQuality
SIO_000300: 7.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.849e-1

GenotypeDepth
all individuals: 35
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6003
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1453
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35365
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1732
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542828931128116e-5
allele num: 64816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11286
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.763e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

FS
type: SiteQuality
SIO_000300: 1.549e0

DP
type: SiteQuality
SIO_000300: 1.402739e6

VQSLOD
type: SiteQuality
SIO_000300: -8.849e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 7.18e0

GenotypeDepth
all individuals: 149
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
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GenotypeQuality
all individuals: 1550
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 923
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6018
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541829843658454e-5
allele num: 64858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.409081e6

FS
type: SiteQuality
SIO_000300: 4.817e0

MQ
type: SiteQuality
SIO_000300: 5.603e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.505e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.424e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
SIO_000300: 2.47e0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 613
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2678
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2692
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1550
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6018
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 218
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1929
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1036
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 9.75e1
variant carriers: 262

GenotypeQuality
all individuals: 36500
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 12
allele frequency: 1.184600197433366e-3
allele num: 10130
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.393665158371041e-3
allele num: 884
num of homozygotes: 0

South Asian
type: Population
allele count: 30
allele frequency: 1.843657817109145e-3
allele num: 16272
num of homozygotes: 1

Latino
type: Population
allele count: 21
allele frequency: 1.859394368691341e-3
allele num: 11294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 141
allele frequency: 2.17398007955842e-3
allele num: 64858
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.405580947798894e-4
allele num: 8314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 57
allele frequency: 8.758451137062077e-3
allele num: 6508
num of homozygotes: 1

MQRankSum
type: SiteQuality
SIO_000300: -1.424e0

MQ
type: SiteQuality
SIO_000300: 5.603e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.409081e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-2

QD
type: SiteQuality
SIO_000300: 2.47e0

FS
type: SiteQuality
SIO_000300: 4.817e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.200000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.505e-1

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

GenotypeQuality
all individuals: 989
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2445
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variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 1414
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variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 1862
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variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 810
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variant carriers: 0

GenotypeQuality
all individuals: 38187
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variant carriers: 0

GenotypeQuality
all individuals: 424
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variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6057
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.202501202501203e-4
allele num: 8316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.23e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

DP
type: SiteQuality
SIO_000300: 1.410995e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

GenotypeDepth
all individuals: 19288
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 660
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1234
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variant carriers: 0

GenotypeQuality
all individuals: 1800
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 239
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1378
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
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variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1556
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6057
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11258
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64648
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.96501284838901e-4
allele num: 10118
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.704e0

VQSLOD
type: SiteQuality
SIO_000300: 7.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

DP
type: SiteQuality
SIO_000300: 1.416787e6

MQ
type: SiteQuality
SIO_000300: 5.834e1

QD
type: SiteQuality
SIO_000300: 1.052e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

FS
type: SiteQuality
SIO_000300: 8.93e-1

GenotypeDepth
all individuals: 8
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
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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
all individuals: 1506
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 1403
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1435
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variant carriers: 0

GenotypeQuality
all individuals: 215
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GenotypeQuality
all individuals: 657
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variant carriers: 1

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

GenotypeQuality
all individuals: 41913
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.838646202282565e-5
allele num: 10164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 1.318e0

QD
type: SiteQuality
SIO_000300: 9.98e0

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-1

DP
type: SiteQuality
SIO_000300: 1.443294e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.553e0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 1444
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 923
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GenotypeQuality
all individuals: 1369
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 44811
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GenotypeQuality
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GenotypeQuality
all individuals: 217
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GenotypeQuality
all individuals: 1236
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
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GenotypeQuality
all individuals: 567
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 6258
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 9.75e1
variant carriers: 1

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.536334306345061e-5
allele num: 65090
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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DP
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InbreedingCoeff
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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SIO_000300: -8.129999999999999e-1

MQ
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SIO_000300: 5.599e1

ReadPosRankSum
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SIO_000300: 1.63e-1

ClippingRankSum
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SIO_000300: -2.71e-1

QD
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SIO_000300: 1.247e1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.109481915933529e-5
allele num: 16368
num of homozygotes: 0

East Asian
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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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African
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BaseQRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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VQSLOD
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Latino
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allele count: 9
allele frequency: 7.890583903208837e-4
allele num: 11406
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.247191011235955e-3
allele num: 890
num of homozygotes: 0

African
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allele count: 256
allele frequency: 2.49609984399376e-2
allele num: 10256
num of homozygotes: 4

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16370
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.609191903819814e-5
allele num: 65710
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8510
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

FS
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SIO_000300: 2.236e0

QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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SIO_000300: 3.1e-2

InbreedingCoeff
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DP
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MQ
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VQSLOD
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BaseQRankSum
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SIO_000300: -1.51e0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 3
allele frequency: 1.824817518248175e-4
allele num: 16440
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
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: 66212
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
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BaseQRankSum
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SIO_000300: -3.538e0

QD
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SIO_000300: 1.22e1

ReadPosRankSum
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SIO_000300: -1.2e-2

MQ
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DP
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MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -1.76e-1

FS
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SIO_000300: 1.564e0

InbreedingCoeff
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SIO_000300: -3.0e-4

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504981488727689e-5
allele num: 66446
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
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MQRankSum
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DP
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

QD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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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 count: 1
allele frequency: 1.504528631179851e-5
allele num: 66466
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Latino
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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FS
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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European (Non-Finnish)
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allele num: 66590
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East Asian
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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European (Non-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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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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QD
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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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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South Asian
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allele frequency: 6.059871530723549e-5
allele num: 16502
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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MQRankSum
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ReadPosRankSum
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FS
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QD
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MQ
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DP
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ClippingRankSum
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 6614
num of homozygotes: 0

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

European (Finnish)
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Latino
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DP
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SIO_000300: 1.531486e6

MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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MQRankSum
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VQSLOD
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.75e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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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European (Non-Finnish)
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African
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South Asian
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Other
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Latino
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BaseQRankSum
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QD
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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SIO_000300: 1.74e-2

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66700
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Latino
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MQ
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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num of homozygotes: 0

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

European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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Latino
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South Asian
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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DP
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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East Asian
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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ReadPosRankSum
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SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.34e1

GenotypeDepth
all individuals: 17
bin: 6.75e1
variant carriers: 2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 1

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1327
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.000420029402058e-5
allele num: 66662
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.532161e6

QD
type: SiteQuality
SIO_000300: 1.271e1

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.56e-1

GenotypeDepth
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.697e0

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

DP
type: SiteQuality
SIO_000300: 1.530768e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.919e1

FS
type: SiteQuality
SIO_000300: 4.605e0

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

GenotypeDepth
all individuals: 15
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 49430
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

QD
type: SiteQuality
SIO_000300: 1.277e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.530299e6

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 1.767e0

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeDepth
all individuals: 101
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeDepth
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 224
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variant carriers: 0

GenotypeQuality
all individuals: 1460
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
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: 16508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.691e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.445e1

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

DP
type: SiteQuality
SIO_000300: 1.530357e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.341e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

GenotypeDepth
all individuals: 67
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23516
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6482
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 49292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

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

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 224
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.777e0

VQSLOD
type: SiteQuality
SIO_000300: 7.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.64e-1

BaseQRankSum
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SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.029e1

DP
type: SiteQuality
SIO_000300: 1.527599e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 8
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GenotypeDepth
all individuals: 83
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variant carriers: 0

GenotypeDepth
all individuals: 5
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1440
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
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: 8638
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.029e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.527599e6

VQSLOD
type: SiteQuality
SIO_000300: 7.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
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SIO_000300: 1.1e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504302304591131e-5
allele num: 66476
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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MQ
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SIO_000300: 6.0e1

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66312
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 9.759906304899473e-5
allele num: 10246
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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QD
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MQ
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ClippingRankSum
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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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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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East Asian
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allele num: 8628
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South Asian
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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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QD
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DP
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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SIO_000300: 5.962e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 11504
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African
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allele num: 10200
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East Asian
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South Asian
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Other
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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QD
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

South Asian
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European (Finnish)
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Other
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East Asian
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African
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European (Non-Finnish)
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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South Asian
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East Asian
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Latino
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African
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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European (Finnish)
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Latino
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allele num: 11404
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DP
type: SiteQuality
SIO_000300: 1.496169e6

QD
type: SiteQuality
SIO_000300: 1.214e1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-2

GenotypeDepth
all individuals: 15
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5973
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1173
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47028
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 305
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.776549060909251e-5
allele num: 11394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

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