8-107718730-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718730
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718730
    reference: chr 8
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.984T>G
  hgvsp: ENST00000442977.2:c.984T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*737T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32956T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.780T>G
  hgvsp: ENST00000497705.1:c.780T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.981T>G
  hgvsp: ENST00000517566.2:c.981T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.122T>G
  hgvsp: ENST00000519415.2:c.122T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.981T>G
  hgvsp: ENST00000445937.1:c.981T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.960T>G
  hgvsp: ENST00000312046.6:c.960T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-550T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.981T>G
  hgvsp: ENST00000531443.1:c.981T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro328Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

8-107718734-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718734
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718734
    reference: chr 8
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*741A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.988A>T
  hgvsp: ENSP00000405424.2:p.Ser330Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.784A>T
  hgvsp: ENSP00000431014.1:p.Ser262Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.964A>T
  hgvsp: ENSP00000311026.6:p.Ser322Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.126A>T
  hgvsp: ENSP00000430701.2:p.Ser43Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-546A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32952A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.985A>T
  hgvsp: ENSP00000402918.1:p.Ser329Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.985A>T
  hgvsp: ENSP00000431966.1:p.Ser329Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.985A>T
  hgvsp: ENSP00000429205.2:p.Ser329Cys
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser330Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

8-107718745-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718745
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718745
    reference: chr 8
allele count: 7
allele frequency: 5.773672055427252e-5
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32941G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-535G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.137G>A
  hgvsp: ENST00000519415.2:c.137G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*752G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.999G>A
  hgvsp: ENST00000442977.2:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.996G>A
  hgvsp: ENST00000445937.1:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.795G>A
  hgvsp: ENST00000497705.1:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.996G>A
  hgvsp: ENST00000531443.1:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.975G>A
  hgvsp: ENST00000312046.6:c.975G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.996G>A
  hgvsp: ENST00000517566.2:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 9.75e1
  variant carriers: 7
hgvs: p.Glu333Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-107718748-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718748
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718748
    reference: chr 8
allele count: 2
allele frequency: 1.649620587264929e-5
allele num: 121240
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1002T>C
  hgvsp: ENST00000442977.2:c.1002T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.999T>C
  hgvsp: ENST00000531443.1:c.999T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.140T>C
  hgvsp: ENST00000519415.2:c.140T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-532T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.999T>C
  hgvsp: ENST00000445937.1:c.999T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*755T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.999T>C
  hgvsp: ENST00000517566.2:c.999T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.978T>C
  hgvsp: ENST00000312046.6:c.978T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.798T>C
  hgvsp: ENST00000497705.1:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32938T>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser334Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

8-107718750-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718750
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718750
    reference: chr 8
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*757T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1001T>C
  hgvsp: ENSP00000402918.1:p.Leu334Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1004T>C
  hgvsp: ENSP00000405424.2:p.Leu335Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1001T>C
  hgvsp: ENSP00000429205.2:p.Leu334Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.800T>C
  hgvsp: ENSP00000431014.1:p.Leu267Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.142T>C
  hgvsp: ENSP00000430701.2:p.Leu48Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.980T>C
  hgvsp: ENSP00000311026.6:p.Leu327Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-530T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1001T>C
  hgvsp: ENSP00000431966.1:p.Leu334Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32936T>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1117
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu335Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

8-107718755-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718755
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718755
    reference: chr 8
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.147G>A
  hgvsp: ENSP00000430701.2:p.Glu50Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1006G>A
  hgvsp: ENSP00000429205.2:p.Glu336Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.985G>A
  hgvsp: ENSP00000311026.6:p.Glu329Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.805G>A
  hgvsp: ENSP00000431014.1:p.Glu269Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32931G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1009G>A
  hgvsp: ENSP00000405424.2:p.Glu337Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1006G>A
  hgvsp: ENSP00000402918.1:p.Glu336Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-525G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1006G>A
  hgvsp: ENSP00000431966.1:p.Glu336Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*762G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu337Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

8-107718761-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718761
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718761
    reference: chr 8
allele count: 3
allele frequency: 2.474390062849507e-5
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1012G>A
  hgvsp: ENSP00000402918.1:p.Val338Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32925G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1012G>A
  hgvsp: ENSP00000429205.2:p.Val338Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1015G>A
  hgvsp: ENSP00000405424.2:p.Val339Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.811G>A
  hgvsp: ENSP00000431014.1:p.Val271Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1012G>A
  hgvsp: ENSP00000431966.1:p.Val338Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.991G>A
  hgvsp: ENSP00000311026.6:p.Val331Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.153G>A
  hgvsp: ENSP00000430701.2:p.Val52Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-519G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*768G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38942
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val339Met
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

8-107718765-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718765
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718765
    reference: chr 8
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.815T>G
  hgvsp: ENSP00000431014.1:p.Phe272Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.995T>G
  hgvsp: ENSP00000311026.6:p.Phe332Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1016T>G
  hgvsp: ENSP00000431966.1:p.Phe339Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1016T>G
  hgvsp: ENSP00000429205.2:p.Phe339Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.157T>G
  hgvsp: ENSP00000430701.2:p.Phe53Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*772T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32921T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1016T>G
  hgvsp: ENSP00000402918.1:p.Phe339Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1019T>G
  hgvsp: ENSP00000405424.2:p.Phe340Cys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-515T>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Phe340Cys
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

8-107718778-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718778
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718778
    reference: chr 8
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.828A>G
  hgvsp: ENST00000497705.1:c.828A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1029A>G
  hgvsp: ENST00000445937.1:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*785A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32908A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1032A>G
  hgvsp: ENST00000442977.2:c.1032A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1008A>G
  hgvsp: ENST00000312046.6:c.1008A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1029A>G
  hgvsp: ENST00000517566.2:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1029A>G
  hgvsp: ENST00000531443.1:c.1029A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-502A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.170A>G
  hgvsp: ENST00000519415.2:c.170A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu344Glu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

8-107718782-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718782
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718782
    reference: chr 8
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.174T>C
  hgvsp: ENSP00000430701.2:p.Ser59Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1033T>C
  hgvsp: ENSP00000431966.1:p.Ser345Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32904T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*789T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1033T>C
  hgvsp: ENSP00000429205.2:p.Ser345Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.832T>C
  hgvsp: ENSP00000431014.1:p.Ser278Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1036T>C
  hgvsp: ENSP00000405424.2:p.Ser346Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1012T>C
  hgvsp: ENSP00000311026.6:p.Ser338Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1033T>C
  hgvsp: ENSP00000402918.1:p.Ser345Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-498T>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser346Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

8-107718787-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718787
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718787
    reference: chr 8
allele count: 2
allele frequency: 1.649783878311941e-5
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-493T>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*794T>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.179T>A
  hgvsp: ENST00000519415.2:c.179T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1038T>A
  hgvsp: ENST00000517566.2:c.1038T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1017T>A
  hgvsp: ENST00000312046.6:c.1017T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1041T>A
  hgvsp: ENST00000442977.2:c.1041T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.837T>A
  hgvsp: ENST00000497705.1:c.837T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1038T>A
  hgvsp: ENST00000445937.1:c.1038T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1038T>A
  hgvsp: ENST00000531443.1:c.1038T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32899T>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5053
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro347Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

8-107718789-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718789
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718789
    reference: chr 8
allele count: 2
allele frequency: 1.649783878311941e-5
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*796T>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.181T>A
  hgvsp: ENSP00000430701.2:p.Ile61Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.839T>A
  hgvsp: ENSP00000431014.1:p.Ile280Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1040T>A
  hgvsp: ENSP00000431966.1:p.Ile347Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1043T>A
  hgvsp: ENSP00000405424.2:p.Ile348Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1019T>A
  hgvsp: ENSP00000311026.6:p.Ile340Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1040T>A
  hgvsp: ENSP00000402918.1:p.Ile347Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32897T>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1040T>A
  hgvsp: ENSP00000429205.2:p.Ile347Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-491T>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51439
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile348Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

8-107718790-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718790
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718790
    reference: chr 8
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.182A>G
  hgvsp: ENSP00000430701.2:p.Ile61Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1041A>G
  hgvsp: ENSP00000429205.2:p.Ile347Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-490A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1041A>G
  hgvsp: ENSP00000402918.1:p.Ile347Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1041A>G
  hgvsp: ENSP00000431966.1:p.Ile347Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32896A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1044A>G
  hgvsp: ENSP00000405424.2:p.Ile348Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1020A>G
  hgvsp: ENSP00000311026.6:p.Ile340Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.840A>G
  hgvsp: ENSP00000431014.1:p.Ile280Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*797A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile348Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

8-107718792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718792
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718792
    reference: chr 8
allele count: 2
allele frequency: 1.649838315845047e-5
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1022G>A
  hgvsp: ENSP00000311026.6:p.Arg341Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1043G>A
  hgvsp: ENSP00000429205.2:p.Arg348Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.842G>A
  hgvsp: ENSP00000431014.1:p.Arg281Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1046G>A
  hgvsp: ENSP00000405424.2:p.Arg349Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-488G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1043G>A
  hgvsp: ENSP00000431966.1:p.Arg348Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.184G>A
  hgvsp: ENSP00000430701.2:p.Arg62Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1043G>A
  hgvsp: ENSP00000402918.1:p.Arg348Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32894G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*799G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51428
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg349Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

8-107718792-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718792
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718792
    reference: chr 8
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.184G>T
  hgvsp: ENSP00000430701.2:p.Arg62Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.842G>T
  hgvsp: ENSP00000431014.1:p.Arg281Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1046G>T
  hgvsp: ENSP00000405424.2:p.Arg349Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-488G>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1043G>T
  hgvsp: ENSP00000429205.2:p.Arg348Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1043G>T
  hgvsp: ENSP00000431966.1:p.Arg348Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1043G>T
  hgvsp: ENSP00000402918.1:p.Arg348Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1022G>T
  hgvsp: ENSP00000311026.6:p.Arg341Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32894G>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*799G>T
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5056
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg349Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-107718801-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718801
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718801
    reference: chr 8
allele count: 6
allele frequency: 4.949678270912391e-5
allele num: 121220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32885T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1055T>G
  hgvsp: ENSP00000405424.2:p.Leu352Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1052T>G
  hgvsp: ENSP00000431966.1:p.Leu351Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1052T>G
  hgvsp: ENSP00000429205.2:p.Leu351Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.193T>G
  hgvsp: ENSP00000430701.2:p.Leu65Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*808T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.851T>G
  hgvsp: ENSP00000431014.1:p.Leu284Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1031T>G
  hgvsp: ENSP00000311026.6:p.Leu344Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-479T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1052T>G
  hgvsp: ENSP00000402918.1:p.Leu351Arg
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu352Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

8-107718805-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718805
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718805
    reference: chr 8
allele count: 67
allele frequency: 5.527414325077961e-4
allele num: 121214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.855A>G
  hgvsp: ENST00000497705.1:c.855A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-475A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1056A>G
  hgvsp: ENST00000445937.1:c.1056A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1059A>G
  hgvsp: ENST00000442977.2:c.1059A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32881A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1056A>G
  hgvsp: ENST00000517566.2:c.1056A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1056A>G
  hgvsp: ENST00000531443.1:c.1056A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1035A>G
  hgvsp: ENST00000312046.6:c.1035A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.197A>G
  hgvsp: ENST00000519415.2:c.197A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*812A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 38868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val353Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

8-107718815-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718815
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718815
    reference: chr 8
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32871G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.207G>A
  hgvsp: ENSP00000430701.2:p.Glu70Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.865G>A
  hgvsp: ENSP00000431014.1:p.Glu289Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-465G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1066G>A
  hgvsp: ENSP00000429205.2:p.Glu356Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1069G>A
  hgvsp: ENSP00000405424.2:p.Glu357Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*822G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1045G>A
  hgvsp: ENSP00000311026.6:p.Glu349Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1066G>A
  hgvsp: ENSP00000402918.1:p.Glu356Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1066G>A
  hgvsp: ENSP00000431966.1:p.Glu356Lys
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17288
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38818
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu357Lys
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

8-107718822-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718822
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718822
    reference: chr 8
allele count: 3
allele frequency: 2.475329218786098e-5
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1052G>A
  hgvsp: ENSP00000311026.6:p.Arg351Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1073G>A
  hgvsp: ENSP00000429205.2:p.Arg358Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1076G>A
  hgvsp: ENSP00000405424.2:p.Arg359Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.214G>A
  hgvsp: ENSP00000430701.2:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*829G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1073G>A
  hgvsp: ENSP00000402918.1:p.Arg358Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1073G>A
  hgvsp: ENSP00000431966.1:p.Arg358Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.872G>A
  hgvsp: ENSP00000431014.1:p.Arg291Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-458G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32864G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg359Gln
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

8-107718828-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718828
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718828
    reference: chr 8
allele count: 2
allele frequency: 1.650110557407346e-5
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1082A>G
  hgvsp: ENSP00000405424.2:p.Asp361Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1058A>G
  hgvsp: ENSP00000311026.6:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32858A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-452A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1079A>G
  hgvsp: ENSP00000402918.1:p.Asp360Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.220A>G
  hgvsp: ENSP00000430701.2:p.Asp74Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.878A>G
  hgvsp: ENSP00000431014.1:p.Asp293Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1079A>G
  hgvsp: ENSP00000431966.1:p.Asp360Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1079A>G
  hgvsp: ENSP00000429205.2:p.Asp360Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*835A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp361Gly
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-107718832-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718832
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718832
    reference: chr 8
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1062A>G
  hgvsp: ENST00000312046.6:c.1062A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-448A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.882A>G
  hgvsp: ENST00000497705.1:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1083A>G
  hgvsp: ENST00000445937.1:c.1083A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32854A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1083A>G
  hgvsp: ENST00000517566.2:c.1083A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.224A>G
  hgvsp: ENST00000519415.2:c.224A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1083A>G
  hgvsp: ENST00000531443.1:c.1083A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1086A>G
  hgvsp: ENST00000442977.2:c.1086A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*839A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51401
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys362Lys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum

8-107718832-ATCT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718832
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718829
    reference: chr 8
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1087_1089delTCT
  hgvsp: ENSP00000431966.1:p.Ser363del
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.886_888delTCT
  hgvsp: ENSP00000431014.1:p.Ser296del
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1066_1068delTCT
  hgvsp: ENSP00000311026.6:p.Ser356del
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1087_1089delTCT
  hgvsp: ENSP00000402918.1:p.Ser363del
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*843_*845delTCT
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1090_1092delTCT
  hgvsp: ENSP00000405424.2:p.Ser364del
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1087_1089delTCT
  hgvsp: ENSP00000429205.2:p.Ser363del
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-444_-442delTCT
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32850_200-32848delTCT
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.228_230delTCT
  hgvsp: ENSP00000430701.2:p.Ser77del
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser364del
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: ATCT
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-107718835-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718835
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718835
    reference: chr 8
allele count: 1
allele frequency: 8.251369727374745e-6
allele num: 121192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-445T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1086T>G
  hgvsp: ENST00000445937.1:c.1086T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1065T>G
  hgvsp: ENST00000312046.6:c.1065T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.227T>G
  hgvsp: ENST00000519415.2:c.227T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*842T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.885T>G
  hgvsp: ENST00000497705.1:c.885T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1086T>G
  hgvsp: ENST00000531443.1:c.1086T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1089T>G
  hgvsp: ENST00000442977.2:c.1089T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32851T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1086T>G
  hgvsp: ENST00000517566.2:c.1086T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17312
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser363Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD

8-107718842-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718842
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718842
    reference: chr 8
allele count: 2
allele frequency: 1.650491846570278e-5
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1096G>A
  hgvsp: ENSP00000405424.2:p.Ala366Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.234G>A
  hgvsp: ENSP00000430701.2:p.Ala79Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1093G>A
  hgvsp: ENSP00000402918.1:p.Ala365Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.892G>A
  hgvsp: ENSP00000431014.1:p.Ala298Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1093G>A
  hgvsp: ENSP00000429205.2:p.Ala365Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1093G>A
  hgvsp: ENSP00000431966.1:p.Ala365Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1072G>A
  hgvsp: ENSP00000311026.6:p.Ala358Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-438G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*849G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32844G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17314
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala366Thr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-107718843-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718843
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718843
    reference: chr 8
allele count: 5
allele frequency: 4.126297720633139e-5
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1094C>T
  hgvsp: ENSP00000429205.2:p.Ala365Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1073C>T
  hgvsp: ENSP00000311026.6:p.Ala358Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32843C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1097C>T
  hgvsp: ENSP00000405424.2:p.Ala366Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.235C>T
  hgvsp: ENSP00000430701.2:p.Ala79Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*850C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1094C>T
  hgvsp: ENSP00000431966.1:p.Ala365Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.893C>T
  hgvsp: ENSP00000431014.1:p.Ala298Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-437C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1094C>T
  hgvsp: ENSP00000402918.1:p.Ala365Val
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala366Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

8-107718844-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718844
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718844
    reference: chr 8
allele count: 5
allele frequency: 4.12609341475491e-5
allele num: 121180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*851G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1095G>A
  hgvsp: ENST00000517566.2:c.1095G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1074G>A
  hgvsp: ENST00000312046.6:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32842G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1095G>A
  hgvsp: ENST00000531443.1:c.1095G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1098G>A
  hgvsp: ENST00000442977.2:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1095G>A
  hgvsp: ENST00000445937.1:c.1095G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.236G>A
  hgvsp: ENST00000519415.2:c.236G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.894G>A
  hgvsp: ENST00000497705.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-436G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala366Ala
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

8-107718845-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718845
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718845
    reference: chr 8
allele count: 52
allele frequency: 4.290924694271615e-4
allele num: 121186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1075T>A
  hgvsp: ENSP00000311026.6:p.Ser359Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1096T>A
  hgvsp: ENSP00000402918.1:p.Ser366Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-435T>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32841T>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1096T>A
  hgvsp: ENSP00000429205.2:p.Ser366Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1099T>A
  hgvsp: ENSP00000405424.2:p.Ser367Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1096T>A
  hgvsp: ENSP00000431966.1:p.Ser366Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.895T>A
  hgvsp: ENSP00000431014.1:p.Ser299Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*852T>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.237T>A
  hgvsp: ENSP00000430701.2:p.Ser80Thr
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser367Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

8-107718845-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718845
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718845
    reference: chr 8
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.237T>C
  hgvsp: ENSP00000430701.2:p.Ser80Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1075T>C
  hgvsp: ENSP00000311026.6:p.Ser359Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*852T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1096T>C
  hgvsp: ENSP00000402918.1:p.Ser366Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1096T>C
  hgvsp: ENSP00000429205.2:p.Ser366Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-435T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.895T>C
  hgvsp: ENSP00000431014.1:p.Ser299Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1099T>C
  hgvsp: ENSP00000405424.2:p.Ser367Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1096T>C
  hgvsp: ENSP00000431966.1:p.Ser366Pro
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32841T>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser367Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/8-107718847-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718847
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718847
    reference: chr 8
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1077A>C
  hgvsp: ENST00000312046.6:c.1077A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.239A>C
  hgvsp: ENST00000519415.2:c.239A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-433A>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1098A>C
  hgvsp: ENST00000517566.2:c.1098A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1098A>C
  hgvsp: ENST00000445937.1:c.1098A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*854A>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.897A>C
  hgvsp: ENST00000497705.1:c.897A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1101A>C
  hgvsp: ENST00000442977.2:c.1101A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1098A>C
  hgvsp: ENST00000531443.1:c.1098A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32839A>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser367Ser
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

8-107718852-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718852
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718852
    reference: chr 8
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.902A>T
  hgvsp: ENSP00000431014.1:p.Glu301Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1106A>T
  hgvsp: ENSP00000405424.2:p.Glu369Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.244A>T
  hgvsp: ENSP00000430701.2:p.Glu82Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1103A>T
  hgvsp: ENSP00000402918.1:p.Glu368Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1103A>T
  hgvsp: ENSP00000431966.1:p.Glu368Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1082A>T
  hgvsp: ENSP00000311026.6:p.Glu361Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32834A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*859A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1103A>T
  hgvsp: ENSP00000429205.2:p.Glu368Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-428A>T
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51420
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu369Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-107718857-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718857
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718857
    reference: chr 8
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1087G>A
  hgvsp: ENSP00000311026.6:p.Val363Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-423G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1111G>A
  hgvsp: ENSP00000405424.2:p.Val371Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1108G>A
  hgvsp: ENSP00000402918.1:p.Val370Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32829G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1108G>A
  hgvsp: ENSP00000431966.1:p.Val370Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*864G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1108G>A
  hgvsp: ENSP00000429205.2:p.Val370Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.907G>A
  hgvsp: ENSP00000431014.1:p.Val303Met
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.249G>A
  hgvsp: ENSP00000430701.2:p.Val84Met
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val371Met
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

8-107718866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718866
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718866
    reference: chr 8
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32820G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1096G>A
  hgvsp: ENSP00000311026.6:p.Val366Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.916G>A
  hgvsp: ENSP00000431014.1:p.Val306Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-414G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1117G>A
  hgvsp: ENSP00000402918.1:p.Val373Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1117G>A
  hgvsp: ENSP00000429205.2:p.Val373Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1120G>A
  hgvsp: ENSP00000405424.2:p.Val374Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1117G>A
  hgvsp: ENSP00000431966.1:p.Val373Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.258G>A
  hgvsp: ENSP00000430701.2:p.Val87Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*873G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51421
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val374Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum

8-107718870-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718870
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718870
    reference: chr 8
allele count: 5
allele frequency: 4.126365827088766e-5
allele num: 121172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1121A>G
  hgvsp: ENSP00000431966.1:p.Asn374Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32816A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1121A>G
  hgvsp: ENSP00000402918.1:p.Asn374Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.920A>G
  hgvsp: ENSP00000431014.1:p.Asn307Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.262A>G
  hgvsp: ENSP00000430701.2:p.Asn88Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*877A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-410A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1100A>G
  hgvsp: ENSP00000311026.6:p.Asn367Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1124A>G
  hgvsp: ENSP00000405424.2:p.Asn375Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1121A>G
  hgvsp: ENSP00000429205.2:p.Asn374Ser
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn375Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP

8-107718877-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718877
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718877
    reference: chr 8
allele count: 1
allele frequency: 8.252323028932645e-6
allele num: 121178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1128T>C
  hgvsp: ENST00000445937.1:c.1128T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1128T>C
  hgvsp: ENST00000531443.1:c.1128T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.927T>C
  hgvsp: ENST00000497705.1:c.927T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32809T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1107T>C
  hgvsp: ENST00000312046.6:c.1107T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1131T>C
  hgvsp: ENST00000442977.2:c.1131T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-403T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*884T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.269T>C
  hgvsp: ENST00000519415.2:c.269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1128T>C
  hgvsp: ENST00000517566.2:c.1128T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17373
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala377Ala
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

8-107718881-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718881
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718881
    reference: chr 8
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*888G>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1132G>C
  hgvsp: ENSP00000402918.1:p.Val378Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1132G>C
  hgvsp: ENSP00000429205.2:p.Val378Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.931G>C
  hgvsp: ENSP00000431014.1:p.Val311Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1135G>C
  hgvsp: ENSP00000405424.2:p.Val379Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.273G>C
  hgvsp: ENSP00000430701.2:p.Val92Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1111G>C
  hgvsp: ENSP00000311026.6:p.Val371Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1132G>C
  hgvsp: ENSP00000431966.1:p.Val378Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32805G>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-399G>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val379Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

8-107718893-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718893
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718893
    reference: chr 8
allele count: 9
allele frequency: 7.427703684141027e-5
allele num: 121168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*900A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1147A>G
  hgvsp: ENSP00000405424.2:p.Thr383Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1144A>G
  hgvsp: ENSP00000402918.1:p.Thr382Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.285A>G
  hgvsp: ENSP00000430701.2:p.Thr96Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.943A>G
  hgvsp: ENSP00000431014.1:p.Thr315Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1144A>G
  hgvsp: ENSP00000429205.2:p.Thr382Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-387A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1144A>G
  hgvsp: ENSP00000431966.1:p.Thr382Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32793A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1123A>G
  hgvsp: ENSP00000311026.6:p.Thr375Ala
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr383Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-107718904-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718904
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718904
    reference: chr 8
allele count: 2
allele frequency: 1.650682557237418e-5
allele num: 121162
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1155A>G
  hgvsp: ENST00000445937.1:c.1155A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1155A>G
  hgvsp: ENST00000531443.1:c.1155A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-376A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*911A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1158A>G
  hgvsp: ENST00000442977.2:c.1158A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32782A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1155A>G
  hgvsp: ENST00000517566.2:c.1155A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.954A>G
  hgvsp: ENST00000497705.1:c.954A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.296A>G
  hgvsp: ENST00000519415.2:c.296A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1134A>G
  hgvsp: ENST00000312046.6:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser386Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

8-107718912-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718912
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718912
    reference: chr 8
allele count: 2
allele frequency: 1.651036851142517e-5
allele num: 121136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1163C>T
  hgvsp: ENSP00000402918.1:p.Thr388Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1142C>T
  hgvsp: ENSP00000311026.6:p.Thr381Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*919C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.304C>T
  hgvsp: ENSP00000430701.2:p.Thr102Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32774C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1163C>T
  hgvsp: ENSP00000429205.2:p.Thr388Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.962C>T
  hgvsp: ENSP00000431014.1:p.Thr321Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-368C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1166C>T
  hgvsp: ENSP00000405424.2:p.Thr389Ile
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1163C>T
  hgvsp: ENSP00000431966.1:p.Thr388Ile
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr389Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

8-107718915-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718915
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718915
    reference: chr 8
allele count: 4
allele frequency: 3.302237265747544e-5
allele num: 121130
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1145G>C
  hgvsp: ENSP00000311026.6:p.Gly382Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*922G>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1169G>C
  hgvsp: ENSP00000405424.2:p.Gly390Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1166G>C
  hgvsp: ENSP00000429205.2:p.Gly389Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.965G>C
  hgvsp: ENSP00000431014.1:p.Gly322Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.307G>C
  hgvsp: ENSP00000430701.2:p.Gly103Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1166G>C
  hgvsp: ENSP00000431966.1:p.Gly389Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32771G>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-365G>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1166G>C
  hgvsp: ENSP00000402918.1:p.Gly389Ala
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly390Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

8-107718920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718920
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718920
    reference: chr 8
allele count: 3
allele frequency: 2.477005135657315e-5
allele num: 121114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*927C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1174C>T
  hgvsp: ENSP00000405424.2:p.Pro392Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1171C>T
  hgvsp: ENSP00000402918.1:p.Pro391Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.970C>T
  hgvsp: ENSP00000431014.1:p.Pro324Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-360C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1171C>T
  hgvsp: ENSP00000431966.1:p.Pro391Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1150C>T
  hgvsp: ENSP00000311026.6:p.Pro384Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.312C>T
  hgvsp: ENSP00000430701.2:p.Pro105Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32766C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1171C>T
  hgvsp: ENSP00000429205.2:p.Pro391Ser
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17397
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro392Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

8-107718944-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718944
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718944
    reference: chr 8
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1195G>A
  hgvsp: ENSP00000402918.1:p.Glu399Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.994G>A
  hgvsp: ENSP00000431014.1:p.Glu332Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1198G>A
  hgvsp: ENSP00000405424.2:p.Glu400Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-336G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1174G>A
  hgvsp: ENSP00000311026.6:p.Glu392Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1195G>A
  hgvsp: ENSP00000431966.1:p.Glu399Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.336G>A
  hgvsp: ENSP00000430701.2:p.Glu113Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1195G>A
  hgvsp: ENSP00000429205.2:p.Glu399Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32742G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*951G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu400Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

8-107718958-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718958
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718958
    reference: chr 8
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1212T>C
  hgvsp: ENST00000442977.2:c.1212T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-322T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1209T>C
  hgvsp: ENST00000517566.2:c.1209T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*965T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32728T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1008T>C
  hgvsp: ENST00000497705.1:c.1008T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1209T>C
  hgvsp: ENST00000445937.1:c.1209T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1209T>C
  hgvsp: ENST00000531443.1:c.1209T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1188T>C
  hgvsp: ENST00000312046.6:c.1188T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.350T>C
  hgvsp: ENST00000519415.2:c.350T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17402
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn404Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-107718967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718967
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718967
    reference: chr 8
allele count: 2
allele frequency: 1.654177625593436e-5
allele num: 120906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1197G>A
  hgvsp: ENST00000312046.6:c.1197G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*974G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1218G>A
  hgvsp: ENST00000445937.1:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1221G>A
  hgvsp: ENST00000442977.2:c.1221G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1218G>A
  hgvsp: ENST00000531443.1:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-313G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1017G>A
  hgvsp: ENST00000497705.1:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1218G>A
  hgvsp: ENST00000517566.2:c.1218G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32719G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.359G>A
  hgvsp: ENST00000519415.2:c.359G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly407Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-107718977-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718977
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718977
    reference: chr 8
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1207C>A
  hgvsp: ENSP00000311026.6:p.His403Asn
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-303C>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1228C>A
  hgvsp: ENSP00000429205.2:p.His410Asn
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1231C>A
  hgvsp: ENSP00000405424.2:p.His411Asn
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1027C>A
  hgvsp: ENSP00000431014.1:p.His343Asn
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*984C>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.369C>A
  hgvsp: ENSP00000430701.2:p.His124Asn
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1228C>A
  hgvsp: ENSP00000402918.1:p.His410Asn
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32709C>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1228C>A
  hgvsp: ENSP00000431966.1:p.His410Asn
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His411Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-107718979-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718979
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718979
    reference: chr 8
allele count: 1
allele frequency: 8.275679433281473e-6
allele num: 120836
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*986T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1029T>G
  hgvsp: ENSP00000431014.1:p.His343Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1230T>G
  hgvsp: ENSP00000429205.2:p.His410Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-301T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32707T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1233T>G
  hgvsp: ENSP00000405424.2:p.His411Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1209T>G
  hgvsp: ENSP00000311026.6:p.His403Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1230T>G
  hgvsp: ENSP00000431966.1:p.His410Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1230T>G
  hgvsp: ENSP00000402918.1:p.His410Gln
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.371T>G
  hgvsp: ENSP00000430701.2:p.His124Gln
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His411Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-107718987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718987
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718987
    reference: chr 8
allele count: 3
allele frequency: 2.484389751064147e-5
allele num: 120754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1037A>G
  hgvsp: ENSP00000431014.1:p.Asp346Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1217A>G
  hgvsp: ENSP00000311026.6:p.Asp406Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1241A>G
  hgvsp: ENSP00000405424.2:p.Asp414Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32699A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1238A>G
  hgvsp: ENSP00000431966.1:p.Asp413Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*994A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-293A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1238A>G
  hgvsp: ENSP00000402918.1:p.Asp413Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.379A>G
  hgvsp: ENSP00000430701.2:p.Asp127Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1238A>G
  hgvsp: ENSP00000429205.2:p.Asp413Gly
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp414Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

8-107718996-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718996
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718996
    reference: chr 8
allele count: 3
allele frequency: 2.485295335929086e-5
allele num: 120710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1247A>G
  hgvsp: ENSP00000402918.1:p.Asn416Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1247A>G
  hgvsp: ENSP00000431966.1:p.Asn416Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1247A>G
  hgvsp: ENSP00000429205.2:p.Asn416Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-284A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1250A>G
  hgvsp: ENSP00000405424.2:p.Asn417Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32690A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1226A>G
  hgvsp: ENSP00000311026.6:p.Asn409Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.388A>G
  hgvsp: ENSP00000430701.2:p.Asn130Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1046A>G
  hgvsp: ENSP00000431014.1:p.Asn349Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1003A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn417Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-107718997-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107718997
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107718997
    reference: chr 8
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1248T>C
  hgvsp: ENST00000517566.2:c.1248T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1047T>C
  hgvsp: ENST00000497705.1:c.1047T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-283T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1251T>C
  hgvsp: ENST00000442977.2:c.1251T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.389T>C
  hgvsp: ENST00000519415.2:c.389T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1248T>C
  hgvsp: ENST00000445937.1:c.1248T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1248T>C
  hgvsp: ENST00000531443.1:c.1248T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1227T>C
  hgvsp: ENST00000312046.6:c.1227T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32689T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1004T>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn417Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

8-107719010-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719010
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719010
    reference: chr 8
allele count: 1
allele frequency: 8.289262089888757e-6
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1240A>G
  hgvsp: ENSP00000311026.6:p.Ile414Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.402A>G
  hgvsp: ENSP00000430701.2:p.Ile135Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-270A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1261A>G
  hgvsp: ENSP00000431966.1:p.Ile421Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32676A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1261A>G
  hgvsp: ENSP00000429205.2:p.Ile421Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1264A>G
  hgvsp: ENSP00000405424.2:p.Ile422Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1261A>G
  hgvsp: ENSP00000402918.1:p.Ile421Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1060A>G
  hgvsp: ENSP00000431014.1:p.Ile354Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1017A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile422Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

8-107719017-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719017
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719017
    reference: chr 8
allele count: 1
allele frequency: 8.293111741387604e-6
allele num: 120582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1268A>T
  hgvsp: ENSP00000429205.2:p.Glu423Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1271A>T
  hgvsp: ENSP00000405424.2:p.Glu424Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1247A>T
  hgvsp: ENSP00000311026.6:p.Glu416Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1268A>T
  hgvsp: ENSP00000402918.1:p.Glu423Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.409A>T
  hgvsp: ENSP00000430701.2:p.Glu137Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32669A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1024A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1268A>T
  hgvsp: ENSP00000431966.1:p.Glu423Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-263A>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1067A>T
  hgvsp: ENSP00000431014.1:p.Glu356Val
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu424Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

8-107719022-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719022
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719022
    reference: chr 8
allele count: 2
allele frequency: 1.659475605708596e-5
allele num: 120520
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.414C>G
  hgvsp: ENSP00000430701.2:p.Gln139Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1273C>G
  hgvsp: ENSP00000402918.1:p.Gln425Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1072C>G
  hgvsp: ENSP00000431014.1:p.Gln358Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1273C>G
  hgvsp: ENSP00000431966.1:p.Gln425Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-258C>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1273C>G
  hgvsp: ENSP00000429205.2:p.Gln425Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32664C>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1276C>G
  hgvsp: ENSP00000405424.2:p.Gln426Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1252C>G
  hgvsp: ENSP00000311026.6:p.Gln418Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1029C>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln426Glu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

8-107719028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719028
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719028
    reference: chr 8
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-252G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1258G>A
  hgvsp: ENSP00000311026.6:p.Ala420Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.420G>A
  hgvsp: ENSP00000430701.2:p.Ala141Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1279G>A
  hgvsp: ENSP00000431966.1:p.Ala427Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1279G>A
  hgvsp: ENSP00000402918.1:p.Ala427Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1279G>A
  hgvsp: ENSP00000429205.2:p.Ala427Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1282G>A
  hgvsp: ENSP00000405424.2:p.Ala428Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1035G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1078G>A
  hgvsp: ENSP00000431014.1:p.Ala360Thr
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32658G>A
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala428Thr
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: G
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/8-107719042-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719042
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719042
    reference: chr 8
allele count: 4
allele frequency: 3.322479898996611e-5
allele num: 120392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1293A>C
  hgvsp: ENSP00000402918.1:p.Gln431His
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32644A>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1293A>C
  hgvsp: ENSP00000431966.1:p.Gln431His
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-238A>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.434A>C
  hgvsp: ENSP00000430701.2:p.Gln145His
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1092A>C
  hgvsp: ENSP00000431014.1:p.Gln364His
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1272A>C
  hgvsp: ENSP00000311026.6:p.Gln424His
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1293A>C
  hgvsp: ENSP00000429205.2:p.Gln431His
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1049A>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1296A>C
  hgvsp: ENSP00000405424.2:p.Gln432His
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln432His
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-107719043-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719043
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719043
    reference: chr 8
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.435G>C
  hgvsp: ENSP00000430701.2:p.Gly146Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1050G>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1273G>C
  hgvsp: ENSP00000311026.6:p.Gly425Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1294G>C
  hgvsp: ENSP00000402918.1:p.Gly432Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32643G>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1297G>C
  hgvsp: ENSP00000405424.2:p.Gly433Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1093G>C
  hgvsp: ENSP00000431014.1:p.Gly365Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1294G>C
  hgvsp: ENSP00000429205.2:p.Gly432Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1294G>C
  hgvsp: ENSP00000431966.1:p.Gly432Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-237G>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly433Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

8-107719049-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719049
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719049
    reference: chr 8
allele count: 1
allele frequency: 8.308684236764266e-6
allele num: 120356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1279T>G
  hgvsp: ENSP00000311026.6:p.Ser427Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32637T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-231T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1300T>G
  hgvsp: ENSP00000402918.1:p.Ser434Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1303T>G
  hgvsp: ENSP00000405424.2:p.Ser435Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1056T>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1099T>G
  hgvsp: ENSP00000431014.1:p.Ser367Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1300T>G
  hgvsp: ENSP00000431966.1:p.Ser434Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1300T>G
  hgvsp: ENSP00000429205.2:p.Ser434Ala
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.441T>G
  hgvsp: ENSP00000430701.2:p.Ser148Ala
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4995
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser435Ala
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

8-107719053-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719053
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719053
    reference: chr 8
allele count: 19
allele frequency: 1.578807418732965e-4
allele num: 120344
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1307G>A
  hgvsp: ENSP00000405424.2:p.Gly436Asp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32633G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-227G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1060G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1103G>A
  hgvsp: ENSP00000431014.1:p.Gly368Asp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1304G>A
  hgvsp: ENSP00000402918.1:p.Gly435Asp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1283G>A
  hgvsp: ENSP00000311026.6:p.Gly428Asp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1304G>A
  hgvsp: ENSP00000429205.2:p.Gly435Asp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1304G>A
  hgvsp: ENSP00000431966.1:p.Gly435Asp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.445G>A
  hgvsp: ENSP00000430701.2:p.Gly149Asp
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly436Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff

8-107719058-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719058
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719058
    reference: chr 8
allele count: 1
allele frequency: 8.30923654734603e-6
allele num: 120348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1288A>G
  hgvsp: ENSP00000311026.6:p.Lys430Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1108A>G
  hgvsp: ENSP00000431014.1:p.Lys370Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1309A>G
  hgvsp: ENSP00000431966.1:p.Lys437Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1309A>G
  hgvsp: ENSP00000402918.1:p.Lys437Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32628A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1309A>G
  hgvsp: ENSP00000429205.2:p.Lys437Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1312A>G
  hgvsp: ENSP00000405424.2:p.Lys438Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.450A>G
  hgvsp: ENSP00000430701.2:p.Lys151Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1065A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-222A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys438Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

8-107719066-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719066
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719066
    reference: chr 8
allele count: 2
allele frequency: 1.661930165694438e-5
allele num: 120342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1317C>T
  hgvsp: ENST00000517566.2:c.1317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1320C>T
  hgvsp: ENST00000442977.2:c.1320C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1317C>T
  hgvsp: ENST00000445937.1:c.1317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1317C>T
  hgvsp: ENST00000531443.1:c.1317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32620C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1116C>T
  hgvsp: ENST00000497705.1:c.1116C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1073C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1296C>T
  hgvsp: ENST00000312046.6:c.1296C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.458C>T
  hgvsp: ENST00000519415.2:c.458C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-214C>T
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3461
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37826
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp440Asp
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/8-107719094-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719094
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719094
    reference: chr 8
allele count: 4
allele frequency: 3.326790645064706e-5
allele num: 120236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32592C>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1345C>A
  hgvsp: ENSP00000429205.2:p.Gln449Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1324C>A
  hgvsp: ENSP00000311026.6:p.Gln442Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-186C>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1345C>A
  hgvsp: ENSP00000402918.1:p.Gln449Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.486C>A
  hgvsp: ENSP00000430701.2:p.Gln163Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1101C>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1348C>A
  hgvsp: ENSP00000405424.2:p.Gln450Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1345C>A
  hgvsp: ENSP00000431966.1:p.Gln449Lys
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1144C>A
  hgvsp: ENSP00000431014.1:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln450Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

8-107719094-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719094
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719094
    reference: chr 8
allele count: 1
allele frequency: 8.316976612661764e-6
allele num: 120236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32592C>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1345C>G
  hgvsp: ENSP00000431966.1:p.Gln449Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1144C>G
  hgvsp: ENSP00000431014.1:p.Gln382Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1348C>G
  hgvsp: ENSP00000405424.2:p.Gln450Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-186C>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.486C>G
  hgvsp: ENSP00000430701.2:p.Gln163Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1324C>G
  hgvsp: ENSP00000311026.6:p.Gln442Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1345C>G
  hgvsp: ENSP00000402918.1:p.Gln449Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1345C>G
  hgvsp: ENSP00000429205.2:p.Gln449Glu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1101C>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln450Glu
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

8-107719104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719104
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719104
    reference: chr 8
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1358T>C
  hgvsp: ENSP00000405424.2:p.Phe453Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32582T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1355T>C
  hgvsp: ENSP00000402918.1:p.Phe452Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1355T>C
  hgvsp: ENSP00000431966.1:p.Phe452Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1154T>C
  hgvsp: ENSP00000431014.1:p.Phe385Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1334T>C
  hgvsp: ENSP00000311026.6:p.Phe445Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1111T>C
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.496T>C
  hgvsp: ENSP00000430701.2:p.Phe166Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1355T>C
  hgvsp: ENSP00000429205.2:p.Phe452Ser
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-176T>C
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4969
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Phe453Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

8-107719114-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719114
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719114
    reference: chr 8
allele count: 2
allele frequency: 1.663948883490299e-5
allele num: 120196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1121G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1344G>A
  hgvsp: ENST00000312046.6:c.1344G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.506G>A
  hgvsp: ENST00000519415.2:c.506G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1365G>A
  hgvsp: ENST00000517566.2:c.1365G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1365G>A
  hgvsp: ENST00000445937.1:c.1365G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-166G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32572G>A
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1368G>A
  hgvsp: ENST00000442977.2:c.1368G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1164G>A
  hgvsp: ENST00000497705.1:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1365G>A
  hgvsp: ENST00000531443.1:c.1365G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu456Glu
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

8-107719119-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719119
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719119
    reference: chr 8
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.511C>G
  hgvsp: ENSP00000430701.2:p.Ser171Trp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1373C>G
  hgvsp: ENSP00000405424.2:p.Ser458Trp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1126C>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-161C>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1169C>G
  hgvsp: ENSP00000431014.1:p.Ser390Trp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1370C>G
  hgvsp: ENSP00000402918.1:p.Ser457Trp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1370C>G
  hgvsp: ENSP00000431966.1:p.Ser457Trp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1370C>G
  hgvsp: ENSP00000429205.2:p.Ser457Trp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1349C>G
  hgvsp: ENSP00000311026.6:p.Ser450Trp
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32567C>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser458Trp
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

8-107719119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719119
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719119
    reference: chr 8
allele count: 1
allele frequency: 8.321405984755183e-6
allele num: 120172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1126C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-161C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.511C>T
  hgvsp: ENSP00000430701.2:p.Ser171Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1370C>T
  hgvsp: ENSP00000429205.2:p.Ser457Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1370C>T
  hgvsp: ENSP00000402918.1:p.Ser457Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1349C>T
  hgvsp: ENSP00000311026.6:p.Ser450Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1169C>T
  hgvsp: ENSP00000431014.1:p.Ser390Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32567C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1373C>T
  hgvsp: ENSP00000405424.2:p.Ser458Leu
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1370C>T
  hgvsp: ENSP00000431966.1:p.Ser457Leu
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser458Leu
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-107719126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719126
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719126
    reference: chr 8
allele count: 1
allele frequency: 8.320990530712775e-6
allele num: 120178
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1380C>T
  hgvsp: ENST00000442977.2:c.1380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-154C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1356C>T
  hgvsp: ENST00000312046.6:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1377C>T
  hgvsp: ENST00000531443.1:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.518C>T
  hgvsp: ENST00000519415.2:c.518C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1377C>T
  hgvsp: ENST00000445937.1:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32560C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1133C>T
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1377C>T
  hgvsp: ENST00000517566.2:c.1377C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1176C>T
  hgvsp: ENST00000497705.1:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His460His
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

8-107719128-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719128
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719128
    reference: chr 8
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.520A>G
  hgvsp: ENSP00000430701.2:p.Gln174Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-152A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1379A>G
  hgvsp: ENSP00000402918.1:p.Gln460Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1358A>G
  hgvsp: ENSP00000311026.6:p.Gln453Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1178A>G
  hgvsp: ENSP00000431014.1:p.Gln393Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32558A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1379A>G
  hgvsp: ENSP00000429205.2:p.Gln460Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1135A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1382A>G
  hgvsp: ENSP00000405424.2:p.Gln461Arg
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1379A>G
  hgvsp: ENSP00000431966.1:p.Gln460Arg
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln461Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

8-107719131-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719131
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719131
    reference: chr 8
allele count: 5
allele frequency: 4.160356792198499e-5
allele num: 120182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1382A>G
  hgvsp: ENSP00000429205.2:p.Glu461Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1385A>G
  hgvsp: ENSP00000405424.2:p.Glu462Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1138A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1382A>G
  hgvsp: ENSP00000402918.1:p.Glu461Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1181A>G
  hgvsp: ENSP00000431014.1:p.Glu394Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.523A>G
  hgvsp: ENSP00000430701.2:p.Glu175Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1361A>G
  hgvsp: ENSP00000311026.6:p.Glu454Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1382A>G
  hgvsp: ENSP00000431966.1:p.Glu461Gly
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-149A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32555A>G
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu462Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

8-107719147-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719147
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719147
    reference: chr 8
allele count: 1
allele frequency: 8.323068215867098e-6
allele num: 120148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1398A>G
  hgvsp: ENST00000531443.1:c.1398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1401A>G
  hgvsp: ENST00000442977.2:c.1401A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-133A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1398A>G
  hgvsp: ENST00000445937.1:c.1398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.539A>G
  hgvsp: ENST00000519415.2:c.539A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1197A>G
  hgvsp: ENST00000497705.1:c.1197A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32539A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1154A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1398A>G
  hgvsp: ENST00000517566.2:c.1398A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1377A>G
  hgvsp: ENST00000312046.6:c.1377A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu467Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

8-107719151-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 107719151
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 107719151
    reference: chr 8
allele count: 2
allele frequency: 1.664669063790118e-5
allele num: 120144
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000405424
  ensembl transcript: ENST00000442977
  gene symbol: OXR1
  hgvsc: ENST00000442977.2:c.1405A>G
  hgvsp: ENSP00000405424.2:p.Met469Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000429205
  ensembl transcript: ENST00000517566
  gene symbol: OXR1
  hgvsc: ENST00000517566.2:c.1402A>G
  hgvsp: ENSP00000429205.2:p.Met468Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000387886
  ensembl transcript: ENST00000435082
  gene symbol: OXR1
  hgvsc: ENST00000435082.1:c.200-32535A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431014
  ensembl transcript: ENST00000497705
  gene symbol: OXR1
  hgvsc: ENST00000497705.1:c.1201A>G
  hgvsp: ENSP00000431014.1:p.Met401Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000414992
  ensembl transcript: ENST00000438229
  gene symbol: OXR1
  hgvsc: ENST00000438229.2:c.*1158A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000431966
  ensembl transcript: ENST00000531443
  gene symbol: OXR1
  hgvsc: ENST00000531443.1:c.1402A>G
  hgvsp: ENSP00000431966.1:p.Met468Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000395032
  ensembl transcript: ENST00000452423
  gene symbol: OXR1
  hgvsc: ENST00000452423.2:c.-129A>G
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000430701
  ensembl transcript: ENST00000519415
  gene symbol: OXR1
  hgvsc: ENST00000519415.2:c.543A>G
  hgvsp: ENSP00000430701.2:p.Met182Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000311026
  ensembl transcript: ENST00000312046
  gene symbol: OXR1
  hgvsc: ENST00000312046.6:c.1381A>G
  hgvsp: ENSP00000311026.6:p.Met461Val
  variant of: http://identifiers.org/hgnc/15822
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000164830
  ensembl protein: ENSP00000402918
  ensembl transcript: ENST00000445937
  gene symbol: OXR1
  hgvsc: ENST00000445937.1:c.1402A>G
  hgvsp: ENSP00000402918.1:p.Met468Val
  variant of: http://identifiers.org/hgnc/15822
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Met469Val
num of homozygotes: 0
reference allele: A

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

GenotypeQuality
all individuals: 619
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5032
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51482
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
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: 11486
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

DP
type: SiteQuality
SIO_000300: 1.459089e6

FS
type: SiteQuality
SIO_000300: 7.122e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.514e0

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: -9.299999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: -4.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.82e-1

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5029
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51454
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

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

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

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 2.522e0

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

DP
type: SiteQuality
SIO_000300: 1.459297e6

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.08e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

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

GenotypeQuality
all individuals: 25
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51471
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5025
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.241396025206011e-4
allele num: 16504
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.18e0

MQRankSum
type: SiteQuality
SIO_000300: 6.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.94e-1

FS
type: SiteQuality
SIO_000300: 2.444e0

QD
type: SiteQuality
SIO_000300: 1.44e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

DP
type: SiteQuality
SIO_000300: 1.459902e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0
bin: 1.25e1
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GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e-1

DP
type: SiteQuality
SIO_000300: 1.45978e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

FS
type: SiteQuality
SIO_000300: 8.99e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 1.48e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.039e0

DP
type: SiteQuality
SIO_000300: 1.459649e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 2.169e1

FS
type: SiteQuality
SIO_000300: 6.856e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.86e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.882e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 462
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5031
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

MQ
type: SiteQuality
SIO_000300: 5.853e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.962e0

FS
type: SiteQuality
SIO_000300: 2.894e0

DP
type: SiteQuality
SIO_000300: 1.45978e6

QD
type: SiteQuality
SIO_000300: 1.409e1

VQSLOD
type: SiteQuality
SIO_000300: -1.58e0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
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: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.075e0

BaseQRankSum
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SIO_000300: -2.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQ
type: SiteQuality
SIO_000300: 5.831e1

ClippingRankSum
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.188e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-1

DP
type: SiteQuality
SIO_000300: 1.459755e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8648
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16502
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 3.5e-3

ReadPosRankSum
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DP
type: SiteQuality
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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MQ
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SIO_000300: 5.979e1

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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11482
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: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999400119976005e-5
allele num: 66680
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 1.429e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.68e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.459974e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.379999999999999e-1

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1116
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 5056
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

FS
type: SiteQuality
SIO_000300: 1.0557e1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

DP
type: SiteQuality
SIO_000300: 1.459961e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.012e1

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

GenotypeQuality
all individuals: 275
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1114
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 1.101e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.015e0

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

DP
type: SiteQuality
SIO_000300: 1.459919e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

QD
type: SiteQuality
SIO_000300: 1.19e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.55e0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5056
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.193e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

DP
type: SiteQuality
SIO_000300: 1.46021e6

FS
type: SiteQuality
SIO_000300: 5.037e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.17e1

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.46021e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.7e-2

FS
type: SiteQuality
SIO_000300: 5.037e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.17e1

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.193e0

GenotypeQuality
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bin: 2.5e0
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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.498050506868214e-5
allele num: 66684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.22e-1

DP
type: SiteQuality
SIO_000300: 1.460137e6

QD
type: SiteQuality
SIO_000300: 1.422e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 67

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

South Asian
type: Population
allele count: 66
allele frequency: 3.999515210277542e-3
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.463617e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e0

QD
type: SiteQuality
SIO_000300: 1.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.107e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

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: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

FS
type: SiteQuality
SIO_000300: 3.834e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.739e0

DP
type: SiteQuality
SIO_000300: 1.461498e6

QD
type: SiteQuality
SIO_000300: 1.206e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.61e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

GenotypeQuality
all individuals: 493
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5053
bin: 6.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999490086685263e-5
allele num: 66678
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.07e-1

QD
type: SiteQuality
SIO_000300: 1.468e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.006e0

DP
type: SiteQuality
SIO_000300: 1.461504e6

FS
type: SiteQuality
SIO_000300: 5.36e0

MQRankSum
type: SiteQuality
SIO_000300: 7.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeQuality
all individuals: 5051
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 624
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variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999310158663508e-5
allele num: 66682
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -6.22e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.103e0

QD
type: SiteQuality
SIO_000300: 1.408e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.08e0

DP
type: SiteQuality
SIO_000300: 1.461482e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeQuality
all individuals: 492
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 262
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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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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: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

FS
type: SiteQuality
SIO_000300: 6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

QD
type: SiteQuality
SIO_000300: 1.674e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.461452e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 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: 11466
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.1e0

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

QD
type: SiteQuality
SIO_000300: 1.674e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

DP
type: SiteQuality
SIO_000300: 1.461452e6

FS
type: SiteQuality
SIO_000300: 6.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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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: 22
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 8
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51385
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

DP
type: SiteQuality
SIO_000300: 1.461537e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.642e0

QD
type: SiteQuality
SIO_000300: 1.542e1

GenotypeQuality
all individuals: 21
bin: 5.75e1
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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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.924557351809084e-4
allele num: 10392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.388e1

DP
type: SiteQuality
SIO_000300: 1.461618e6

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 4.785e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.712e0

MQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.79e-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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variant carriers: 5

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
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.724480893386844e-5
allele num: 11462
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.818402230573403e-4
allele num: 16498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

FS
type: SiteQuality
SIO_000300: 1.093e0

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.145e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

DP
type: SiteQuality
SIO_000300: 1.461853e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.76e-1

QD
type: SiteQuality
SIO_000300: 1.2e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
bin: 4.25e1
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GenotypeQuality
all individuals: 261
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GenotypeQuality
all individuals: 275
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GenotypeQuality
all individuals: 37
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.75e1
variant carriers: 5

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

Other
type: Population
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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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European (Finnish)
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allele frequency: 3.027550711474417e-4
allele num: 6606
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 4.499640028797696e-5
allele num: 66672
num of homozygotes: 0

FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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SIO_000300: 5.981e1

ClippingRankSum
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DP
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BaseQRankSum
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SIO_000300: 1.94e0

ReadPosRankSum
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SIO_000300: 9.03e-1

QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 5.898681471200555e-3
allele num: 8646
num of homozygotes: 0

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

FS
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BaseQRankSum
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QD
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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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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16500
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
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allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

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

ReadPosRankSum
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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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SIO_000300: 2.0e-3

FS
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MQ
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SIO_000300: 5.96e1

VQSLOD
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QD
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SIO_000300: 1.259e1

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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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

South Asian
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ReadPosRankSum
type: SiteQuality
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QD
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MQ
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SIO_000300: 5.929e1

InbreedingCoeff
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VQSLOD
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FS
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DP
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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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
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66674
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South Asian
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allele frequency: 6.06060606060606e-5
allele num: 16500
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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Other
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BaseQRankSum
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MQ
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DP
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QD
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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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
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Other
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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: 1.499970000599988e-5
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South Asian
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6606
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African
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East Asian
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FS
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VQSLOD
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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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
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variant carriers: 0

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

African
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Other
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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MQ
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SIO_000300: 5.912e1

BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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DP
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QD
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.50030001200048e-5
allele num: 66664
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South Asian
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Other
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MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5029
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 2.866e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.086e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.46211e6

MQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-1

QD
type: SiteQuality
SIO_000300: 1.631e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 9.23e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 1.462119e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

QD
type: SiteQuality
SIO_000300: 1.422e1

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 5023
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 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: 11462
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.455206691720208e-4
allele num: 16498
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

QD
type: SiteQuality
SIO_000300: 1.459e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.63e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.67e0

DP
type: SiteQuality
SIO_000300: 1.462392e6

GenotypeQuality
all individuals: 1157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 496
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5024
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000030000300003e-5
allele num: 66666
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.424e1

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.46196e6

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

FS
type: SiteQuality
SIO_000300: 4.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.6e-2

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

GenotypeQuality
all individuals: 1111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 8.25e1
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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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
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.301e0

DP
type: SiteQuality
SIO_000300: 1.461622e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

QD
type: SiteQuality
SIO_000300: 1.237e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.223e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5009
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.860258637328701e-4
allele num: 10362
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 5.879e0

DP
type: SiteQuality
SIO_000300: 1.461849e6

QD
type: SiteQuality
SIO_000300: 1.426e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5007
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818622696411251e-4
allele num: 16496
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

FS
type: SiteQuality
SIO_000300: 7.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.46149e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.74e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.963e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-2

QD
type: SiteQuality
SIO_000300: 1.53e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51172
bin: 6.25e1
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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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
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 498
bin: 9.75e1
variant carriers: 1

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.05e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.073e0

DP
type: SiteQuality
SIO_000300: 1.460296e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.468e0

QD
type: SiteQuality
SIO_000300: 1.254e1

GenotypeQuality
all individuals: 271
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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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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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51138
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.565e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

DP
type: SiteQuality
SIO_000300: 1.459831e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.69e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.351e0

QD
type: SiteQuality
SIO_000300: 4.04e0

MQRankSum
type: SiteQuality
SIO_000300: -6.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.883e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00318337437684e-5
allele num: 66596
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 2.496e0

DP
type: SiteQuality
SIO_000300: 1.459424e6

QD
type: SiteQuality
SIO_000300: 1.12e1

VQSLOD
type: SiteQuality
SIO_000300: -6.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.216e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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: 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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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.11e-1

MQ
type: SiteQuality
SIO_000300: 5.858e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.576e0

QD
type: SiteQuality
SIO_000300: 7.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.012e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.598e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.458849e6

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10188
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.31e0

FS
type: SiteQuality
SIO_000300: 8.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 4.19e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.714e1

DP
type: SiteQuality
SIO_000300: 1.458432e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-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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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.509379509379509e-5
allele num: 66528
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.56e0

QD
type: SiteQuality
SIO_000300: 1.566e1

MQRankSum
type: SiteQuality
SIO_000300: -1.229e0

DP
type: SiteQuality
SIO_000300: 1.457819e6

FS
type: SiteQuality
SIO_000300: 1.028e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.825e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.147e0

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: 6602
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.511549566891241e-5
allele num: 66496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 4.13e-1

QD
type: SiteQuality
SIO_000300: 1.459e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 904
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.848335631278314e-5
allele num: 10154
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66496
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.907e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 1.8e-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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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50886
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.744316194473592e-5
allele num: 11436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.403e0

QD
type: SiteQuality
SIO_000300: 1.427e1

FS
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

DP
type: SiteQuality
SIO_000300: 1.456394e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

GenotypeQuality
all individuals: 263
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66394
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.456002e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.931e0

MQRankSum
type: SiteQuality
SIO_000300: -2.023e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.624e0

QD
type: SiteQuality
SIO_000300: 6.71e0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.014408874419726e-5
allele num: 66348
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

DP
type: SiteQuality
SIO_000300: 1.455729e6

FS
type: SiteQuality
SIO_000300: 8.965e0

VQSLOD
type: SiteQuality
SIO_000300: -6.634e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.59e-1

QD
type: SiteQuality
SIO_000300: 1.718e1

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50839
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.074596039363382e-5
allele num: 16462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

QD
type: SiteQuality
SIO_000300: 1.376e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.011e0

MQRankSum
type: SiteQuality
SIO_000300: -2.362e0

DP
type: SiteQuality
SIO_000300: 1.455614e6

FS
type: SiteQuality
SIO_000300: 7.451e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
all individuals: 5000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 577
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GenotypeQuality
all individuals: 1107
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GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 50710
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variant carriers: 0

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11416
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.863878477017163e-5
allele num: 10138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.527755139002083e-5
allele num: 66258
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.904e0

FS
type: SiteQuality
SIO_000300: 1.719e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 1.484e1

DP
type: SiteQuality
SIO_000300: 1.454665e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.699999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.914e1

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: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50934283213089e-5
allele num: 66254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.453e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.330000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
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SIO_000300: -2.692e0

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

DP
type: SiteQuality
SIO_000300: 1.454701e6

FS
type: SiteQuality
SIO_000300: 4.887e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.02e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.859988168014199e-5
allele num: 10142
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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66230
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.81e-1

MQ
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -3.82e-1

GenotypeQuality
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variant carriers: 19

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 19
allele frequency: 2.206736353077816e-3
allele num: 8610
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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FS
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QD
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DP
type: SiteQuality
SIO_000300: 1.455361e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 263
bin: 9.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510254628930438e-5
allele num: 66214
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.436e1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66206
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.32396002788752e-4
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11404
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

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

BaseQRankSum
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SIO_000300: -1.628e0

InbreedingCoeff
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SIO_000300: -5.0e-4

FS
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DP
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SIO_000300: 1.454079e6

ReadPosRankSum
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SIO_000300: -5.3e-2

QD
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ClippingRankSum
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SIO_000300: 1.7e0

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66144
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.51000351000351e-4
allele num: 11396
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

FS
type: SiteQuality
SIO_000300: 1.2336e1

DP
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SIO_000300: 1.453753e6

InbreedingCoeff
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MQ
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SIO_000300: 5.925e1

MQRankSum
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SIO_000300: 7.82e-1

ClippingRankSum
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SIO_000300: -3.22e-1

VQSLOD
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SIO_000300: -1.64e0

QD
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SIO_000300: 1.158e1

BaseQRankSum
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SIO_000300: -1.867e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 614
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.775008775008775e-5
allele num: 11396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66144
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.2336e1

BaseQRankSum
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SIO_000300: -1.867e0

VQSLOD
type: SiteQuality
SIO_000300: -1.64e0

MQRankSum
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DP
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SIO_000300: 1.453753e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10150
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.085686465433301e-5
allele num: 16432
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.77e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

DP
type: SiteQuality
SIO_000300: 1.453655e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
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SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.61e-1

FS
type: SiteQuality
SIO_000300: 9.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512310205069264e-5
allele num: 66124
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.781173164734808e-5
allele num: 11388
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.882e0

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 1.454242e6

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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variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16426
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.882e1

BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
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DP
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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VQSLOD
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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
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
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: 16426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

MQ
type: SiteQuality
SIO_000300: 5.882e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

FS
type: SiteQuality
SIO_000300: 1.295e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

DP
type: SiteQuality
SIO_000300: 1.454375e6

QD
type: SiteQuality
SIO_000300: 1.329e1

GenotypeQuality
all individuals: 50578
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512355948095944e-5
allele num: 66122
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.135e0

QD
type: SiteQuality
SIO_000300: 1.064e1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 1.454133e6

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.218e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.46e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4958
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 496
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1103
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50587
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512447442451375e-5
allele num: 66118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

DP
type: SiteQuality
SIO_000300: 1.45397e6

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.02e-1

QD
type: SiteQuality
SIO_000300: 1.094e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 8.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e-1

GenotypeQuality
all individuals: 616
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50484
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.562237212256874e-5
allele num: 66118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
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: 8582
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

FS
type: SiteQuality
SIO_000300: 6.378e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.23e0

QD
type: SiteQuality
SIO_000300: 1.222e1

DP
type: SiteQuality
SIO_000300: 1.453908e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4945
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50363
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-5
allele num: 66100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

DP
type: SiteQuality
SIO_000300: 1.452874e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

FS
type: SiteQuality
SIO_000300: 2.255e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.622e1