1-168059862-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059862
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059862
    reference: chr 1
allele count: 8
allele frequency: 7.006358270130143e-5
allele num: 114182
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.802C>A
  hgvsp: ENSP00000444348.1:p.Gln268Lys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1144C>A
  hgvsp: ENSP00000271357.5:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.748C>A
  hgvsp: ENSP00000356810.1:p.Gln250Lys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1144C>A
  hgvsp: ENSP00000356812.1:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1203C>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1144C>A
  hgvsp: ENSP00000355194.2:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1204C>A
  hgvsp: ENSP00000441039.1:p.Gln402Lys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1144C>A
  hgvsp: ENSP00000356809.1:p.Gln382Lys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.910C>A
  hgvsp: ENSP00000437576.1:p.Gln304Lys
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32947
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3838
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 7.75e1
  variant carriers: 1
hgvs: p.Gln402Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

1-168059863-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059863
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059863
    reference: chr 1
allele count: 9
allele frequency: 8.121131183339048e-5
allele num: 110822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1143A>G
  hgvsp: ENST00000271357.5:c.1143A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1202A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.909A>G
  hgvsp: ENST00000539777.1:c.909A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.801A>G
  hgvsp: ENST00000546300.1:c.801A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.747A>G
  hgvsp: ENST00000367836.1:c.747A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1143A>G
  hgvsp: ENST00000361697.2:c.1143A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1143A>G
  hgvsp: ENST00000367835.1:c.1143A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1203A>G
  hgvsp: ENST00000537209.1:c.1203A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1143A>G
  hgvsp: ENST00000367838.1:c.1143A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3843
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32454
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10910
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly401Gly
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

1-168059865-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059865
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059865
    reference: chr 1
allele count: 1
allele frequency: 8.530385232197085e-6
allele num: 117228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.907G>A
  hgvsp: ENSP00000437576.1:p.Gly303Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1141G>A
  hgvsp: ENSP00000271357.5:p.Gly381Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1201G>A
  hgvsp: ENSP00000441039.1:p.Gly401Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1141G>A
  hgvsp: ENSP00000356812.1:p.Gly381Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1141G>A
  hgvsp: ENSP00000355194.2:p.Gly381Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1141G>A
  hgvsp: ENSP00000356809.1:p.Gly381Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.799G>A
  hgvsp: ENSP00000444348.1:p.Gly267Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1200G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.745G>A
  hgvsp: ENSP00000356810.1:p.Gly249Arg
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33574
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly401Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-168059865-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059865
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059864
    reference: chr 1
allele count: 1
allele frequency: 8.530385232197085e-6
allele num: 117228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.906delT
  hgvsp: ENSP00000437576.1:p.Gly303AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.798delT
  hgvsp: ENSP00000444348.1:p.Gly267AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1140delT
  hgvsp: ENSP00000356812.1:p.Gly381AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1140delT
  hgvsp: ENSP00000356809.1:p.Gly381AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1140delT
  hgvsp: ENSP00000355194.2:p.Gly381AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1200delT
  hgvsp: ENSP00000441039.1:p.Gly401AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.744delT
  hgvsp: ENSP00000356810.1:p.Gly249AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1140delT
  hgvsp: ENSP00000271357.5:p.Gly381AspfsTer25
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1199delT
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly401AspfsTer25
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: CA
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/1-168059866-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059866
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059866
    reference: chr 1
allele count: 1991
allele frequency: 1.872754293884155e-2
allele num: 106314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1140T>G
  hgvsp: ENST00000271357.5:c.1140T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.744T>G
  hgvsp: ENST00000367836.1:c.744T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1200T>G
  hgvsp: ENST00000537209.1:c.1200T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.906T>G
  hgvsp: ENST00000539777.1:c.906T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1140T>G
  hgvsp: ENST00000361697.2:c.1140T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1140T>G
  hgvsp: ENST00000367835.1:c.1140T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1199T>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.798T>G
  hgvsp: ENST00000546300.1:c.798T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1140T>G
  hgvsp: ENST00000367838.1:c.1140T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 1.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 2.75e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 5.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 1.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 19183
  bin: 2.25e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 3.25e1
  variant carriers: 283
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.25e1
  variant carriers: 254
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 5.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 4.75e1
  variant carriers: 199
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 5.25e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 2.5e0
  variant carriers: 70
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 1.25e1
  variant carriers: 80
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 6.75e1
  variant carriers: 50
hgvs: p.Gly400Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

1-168059866-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059866
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059866
    reference: chr 1
allele count: 37628
allele frequency: 3.539326899561676e-1
allele num: 106314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1140T>C
  hgvsp: ENST00000367838.1:c.1140T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.744T>C
  hgvsp: ENST00000367836.1:c.744T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1140T>C
  hgvsp: ENST00000367835.1:c.1140T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.798T>C
  hgvsp: ENST00000546300.1:c.798T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1140T>C
  hgvsp: ENST00000271357.5:c.1140T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1140T>C
  hgvsp: ENST00000361697.2:c.1140T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1200T>C
  hgvsp: ENST00000537209.1:c.1200T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.906T>C
  hgvsp: ENST00000539777.1:c.906T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1199T>C
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 6.25e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 9935
  bin: 2.75e1
  variant carriers: 4708
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.5e0
  variant carriers: 1263
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 6150
  bin: 1.75e1
  variant carriers: 4922
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.25e1
  variant carriers: 2313
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 4.75e1
  variant carriers: 1484
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 1.25e1
  variant carriers: 3327
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 5.75e1
  variant carriers: 549
genotype depth: GenotypeDepth
  all individuals: 5840
  bin: 3.25e1
  variant carriers: 3902
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 5.25e1
  variant carriers: 903
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 19183
  bin: 2.25e1
  variant carriers: 5186
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 3113
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 113
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 4.75e1
  variant carriers: 945
genotype quality: GenotypeQuality
  all individuals: 3509
  bin: 2.5e0
  variant carriers: 220
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 3.25e1
  variant carriers: 848
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.75e1
  variant carriers: 600
hgvs: p.Gly400Gly
num of homozygotes: 7239
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

1-168059869-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059869
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059869
    reference: chr 1
allele count: 3
allele frequency: 2.55388701603841e-5
allele num: 117468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1137A>G
  hgvsp: ENST00000367835.1:c.1137A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.741A>G
  hgvsp: ENST00000367836.1:c.741A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.903A>G
  hgvsp: ENST00000539777.1:c.903A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1197A>G
  hgvsp: ENST00000537209.1:c.1197A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1137A>G
  hgvsp: ENST00000271357.5:c.1137A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1137A>G
  hgvsp: ENST00000367838.1:c.1137A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1137A>G
  hgvsp: ENST00000361697.2:c.1137A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.795A>G
  hgvsp: ENST00000546300.1:c.795A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1196A>G
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1267
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala399Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

1-168059878-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059878
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059878
    reference: chr 1
allele count: 6
allele frequency: 5.150303009493726e-5
allele num: 116498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1128G>A
  hgvsp: ENST00000367835.1:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.732G>A
  hgvsp: ENST00000367836.1:c.732G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1188G>A
  hgvsp: ENST00000537209.1:c.1188G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1187G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1128G>A
  hgvsp: ENST00000271357.5:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.786G>A
  hgvsp: ENST00000546300.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1128G>A
  hgvsp: ENST00000361697.2:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1128G>A
  hgvsp: ENST00000367838.1:c.1128G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.894G>A
  hgvsp: ENST00000539777.1:c.894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24420
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala396Ala
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

1-168059879-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059879
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059879
    reference: chr 1
allele count: 20
allele frequency: 1.721081527631964e-4
allele num: 116206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1127C>T
  hgvsp: ENSP00000271357.5:p.Ala376Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.785C>T
  hgvsp: ENSP00000444348.1:p.Ala262Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.731C>T
  hgvsp: ENSP00000356810.1:p.Ala244Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1127C>T
  hgvsp: ENSP00000356812.1:p.Ala376Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1127C>T
  hgvsp: ENSP00000356809.1:p.Ala376Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.893C>T
  hgvsp: ENSP00000437576.1:p.Ala298Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1187C>T
  hgvsp: ENSP00000441039.1:p.Ala396Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1186C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1127C>T
  hgvsp: ENSP00000355194.2:p.Ala376Val
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22936
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24333
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala396Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/1-168059881-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059881
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059881
    reference: chr 1
allele count: 1
allele frequency: 8.615193755707565e-6
allele num: 116074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1184T>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1125T>G
  hgvsp: ENST00000271357.5:c.1125T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1125T>G
  hgvsp: ENST00000367838.1:c.1125T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.783T>G
  hgvsp: ENST00000546300.1:c.783T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1125T>G
  hgvsp: ENST00000361697.2:c.1125T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1125T>G
  hgvsp: ENST00000367835.1:c.1125T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.729T>G
  hgvsp: ENST00000367836.1:c.729T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1185T>G
  hgvsp: ENST00000537209.1:c.1185T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.891T>G
  hgvsp: ENST00000539777.1:c.891T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22986
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr395Thr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

1-168059882-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059882
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059882
    reference: chr 1
allele count: 3
allele frequency: 2.59511081123164e-5
allele num: 115602
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.890C>T
  hgvsp: ENSP00000437576.1:p.Thr297Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1124C>T
  hgvsp: ENSP00000271357.5:p.Thr375Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1124C>T
  hgvsp: ENSP00000356809.1:p.Thr375Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1184C>T
  hgvsp: ENSP00000441039.1:p.Thr395Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.782C>T
  hgvsp: ENSP00000444348.1:p.Thr261Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1124C>T
  hgvsp: ENSP00000356812.1:p.Thr375Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1183C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1124C>T
  hgvsp: ENSP00000355194.2:p.Thr375Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.728C>T
  hgvsp: ENSP00000356810.1:p.Thr243Ile
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24175
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr395Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS

1-168059887-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059887
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059887
    reference: chr 1
allele count: 1
allele frequency: 8.738050715646353e-6
allele num: 114442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1178C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1119C>T
  hgvsp: ENST00000361697.2:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1119C>T
  hgvsp: ENST00000271357.5:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.885C>T
  hgvsp: ENST00000539777.1:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.777C>T
  hgvsp: ENST00000546300.1:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1179C>T
  hgvsp: ENST00000537209.1:c.1179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1119C>T
  hgvsp: ENST00000367838.1:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.723C>T
  hgvsp: ENST00000367836.1:c.723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1119C>T
  hgvsp: ENST00000367835.1:c.1119C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44356
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
hgvs: p.His393His
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

1-168059888-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059888
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059888
    reference: chr 1
allele count: 1
allele frequency: 8.772545441785388e-6
allele num: 113992
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1118A>G
  hgvsp: ENSP00000356812.1:p.His373Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.722A>G
  hgvsp: ENSP00000356810.1:p.His241Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1118A>G
  hgvsp: ENSP00000356809.1:p.His373Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.776A>G
  hgvsp: ENSP00000444348.1:p.His259Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1178A>G
  hgvsp: ENSP00000441039.1:p.His393Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1177A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1118A>G
  hgvsp: ENSP00000271357.5:p.His373Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.884A>G
  hgvsp: ENSP00000437576.1:p.His295Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1118A>G
  hgvsp: ENSP00000355194.2:p.His373Arg
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6213
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4693
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His393Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-168059889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059889
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059889
    reference: chr 1
allele count: 2
allele frequency: 1.764104011572522e-5
allele num: 113372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1117C>T
  hgvsp: ENSP00000356809.1:p.His373Tyr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.775C>T
  hgvsp: ENSP00000444348.1:p.His259Tyr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1117C>T
  hgvsp: ENSP00000271357.5:p.His373Tyr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1117C>T
  hgvsp: ENSP00000355194.2:p.His373Tyr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.883C>T
  hgvsp: ENSP00000437576.1:p.His295Tyr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1176C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.721C>T
  hgvsp: ENSP00000356810.1:p.His241Tyr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1117C>T
  hgvsp: ENSP00000356812.1:p.His373Tyr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1177C>T
  hgvsp: ENSP00000441039.1:p.His393Tyr
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21439
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 42693
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His393Tyr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

1-168059891-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059891
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059891
    reference: chr 1
allele count: 1
allele frequency: 8.849087659062351e-6
allele num: 113006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.719C>A
  hgvsp: ENSP00000356810.1:p.Pro240Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.881C>A
  hgvsp: ENSP00000437576.1:p.Pro294Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1175C>A
  hgvsp: ENSP00000441039.1:p.Pro392Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1115C>A
  hgvsp: ENSP00000356812.1:p.Pro372Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1115C>A
  hgvsp: ENSP00000356809.1:p.Pro372Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1115C>A
  hgvsp: ENSP00000271357.5:p.Pro372Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1115C>A
  hgvsp: ENSP00000355194.2:p.Pro372Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1174C>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.773C>A
  hgvsp: ENSP00000444348.1:p.Pro258Gln
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21349
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro392Gln
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

1-168059905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059905
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059905
    reference: chr 1
allele count: 1
allele frequency: 9.589934404848671e-6
allele num: 104276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1101C>T
  hgvsp: ENST00000271357.5:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.705C>T
  hgvsp: ENST00000367836.1:c.705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1161C>T
  hgvsp: ENST00000537209.1:c.1161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1160C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.867C>T
  hgvsp: ENST00000539777.1:c.867C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1101C>T
  hgvsp: ENST00000367835.1:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1101C>T
  hgvsp: ENST00000367838.1:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.759C>T
  hgvsp: ENST00000546300.1:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1101C>T
  hgvsp: ENST00000361697.2:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17037
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32407
  bin: 6.25e1
  variant carriers: 0
hgvs: c.1161C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-168059920-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059920
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059920
    reference: chr 1
allele count: 4
allele frequency: 4.187166335182665e-5
allele num: 95530
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1160-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.704-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1100-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1159-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.866-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.758-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1100-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1100-14A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1100-14A>G
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9051
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1530
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17895
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

1-168059935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059935
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059935
    reference: chr 1
allele count: 1
allele frequency: 1.163521280804226e-5
allele num: 85946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1100-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.758-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1159-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.866-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1100-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1160-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1100-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.704-29G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1100-29G>A
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28676
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3423
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31555
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-168059938-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059938
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059938
    reference: chr 1
allele count: 1
allele frequency: 1.194600406164138e-5
allele num: 83710
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.866-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1100-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.704-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1160-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.758-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1100-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1159-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1100-32A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1100-32A>G
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28505
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

1-168059941-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059941
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059941
    reference: chr 1
allele count: 4
allele frequency: 4.994131895023347e-5
allele num: 80094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.758-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1100-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1100-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1100-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.704-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.866-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1159-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1160-35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1100-35G>A
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16040
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 6029
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

1-168059952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168059952
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168059952
    reference: chr 1
allele count: 1
allele frequency: 1.488671212076101e-5
allele num: 67174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1100-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1159-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1100-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1160-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1100-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1100-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.866-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.758-46C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.704-46C>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21732
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5643
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4365
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

1-168065700-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065700
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065700
    reference: chr 1
allele count: 2
allele frequency: 1.780912183220245e-5
allele num: 112302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+46C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+46C>G
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13929
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

1-168065711-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065711
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065711
    reference: chr 1
allele count: 1
allele frequency: 8.88509791377901e-6
allele num: 112548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+35G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+35G>A
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13295
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3907
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

1-168065715-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065715
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065715
    reference: chr 1
allele count: 8
allele frequency: 7.085289168364183e-5
allele num: 112910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+31C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+31C>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12276
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4807
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3931
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7600
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

1-168065724-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065724
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065724
    reference: chr 1
allele count: 5
allele frequency: 4.400788621320941e-5
allele num: 113616
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+22T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+22T>C
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4849
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-168065738-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065738
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065738
    reference: chr 1
allele count: 43
allele frequency: 3.716508210890233e-4
allele num: 115700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+8G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+8G>C
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12365
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14484
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1159+8G>C
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

1-168065738-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065738
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065738
    reference: chr 1
allele count: 10
allele frequency: 8.643042350907519e-5
allele num: 115700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+8G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+8G>A
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13318
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2750
  bin: 2.25e1
  variant carriers: 0
hgvs: c.1159+8G>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

1-168065742-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065742
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065742
    reference: chr 1
allele count: 1
allele frequency: 8.596382642184169e-6
allele num: 116328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+4A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+4A>G
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2514
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1159+4A>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: T
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

1-168065743-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065743
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065742
    reference: chr 1
allele count: 1
allele frequency: 8.581333882538702e-6
allele num: 116532
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.757+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.865+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1099+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.703+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1158+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1159+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1099+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1099+2delT
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1099+2delT
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4857
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2437
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3992
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1159+2delT
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: TA
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-168065757-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065757
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065757
    reference: chr 1
allele count: 1
allele frequency: 8.431418839162254e-6
allele num: 118604
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.692A>G
  hgvsp: ENSP00000356810.1:p.Asn231Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1088A>G
  hgvsp: ENSP00000356809.1:p.Asn363Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1147A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1088A>G
  hgvsp: ENSP00000271357.5:p.Asn363Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1088A>G
  hgvsp: ENSP00000355194.2:p.Asn363Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1148A>G
  hgvsp: ENSP00000441039.1:p.Asn383Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.854A>G
  hgvsp: ENSP00000437576.1:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.746A>G
  hgvsp: ENSP00000444348.1:p.Asn249Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1088A>G
  hgvsp: ENSP00000356812.1:p.Asn363Ser
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4019
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn383Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

1-168065778-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065778
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065778
    reference: chr 1
allele count: 1
allele frequency: 8.288025460814215e-6
allele num: 120656
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.833C>G
  hgvsp: ENSP00000437576.1:p.Ser278Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1067C>G
  hgvsp: ENSP00000271357.5:p.Ser356Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1126C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.671C>G
  hgvsp: ENSP00000356810.1:p.Ser224Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.725C>G
  hgvsp: ENSP00000444348.1:p.Ser242Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1127C>G
  hgvsp: ENSP00000441039.1:p.Ser376Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1067C>G
  hgvsp: ENSP00000356809.1:p.Ser356Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1067C>G
  hgvsp: ENSP00000355194.2:p.Ser356Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1067C>G
  hgvsp: ENSP00000356812.1:p.Ser356Cys
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15342
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4049
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser376Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

1-168065790-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065790
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065790
    reference: chr 1
allele count: 2
allele frequency: 1.652237129072764e-5
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1055G>A
  hgvsp: ENSP00000356812.1:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1055G>A
  hgvsp: ENSP00000356809.1:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1114G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.659G>A
  hgvsp: ENSP00000356810.1:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1115G>A
  hgvsp: ENSP00000441039.1:p.Arg372Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.821G>A
  hgvsp: ENSP00000437576.1:p.Arg274Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.713G>A
  hgvsp: ENSP00000444348.1:p.Arg238Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1055G>A
  hgvsp: ENSP00000271357.5:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1055G>A
  hgvsp: ENSP00000355194.2:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8077
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4051
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg372Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/1-168065797-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065797
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065797
    reference: chr 1
allele count: 2
allele frequency: 1.649811096629436e-5
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.814G>T
  hgvsp: ENSP00000437576.1:p.Val272Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.652G>T
  hgvsp: ENSP00000356810.1:p.Val218Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1048G>T
  hgvsp: ENSP00000356812.1:p.Val350Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1048G>T
  hgvsp: ENSP00000356809.1:p.Val350Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1048G>T
  hgvsp: ENSP00000355194.2:p.Val350Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.706G>T
  hgvsp: ENSP00000444348.1:p.Val236Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1108G>T
  hgvsp: ENSP00000441039.1:p.Val370Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1048G>T
  hgvsp: ENSP00000271357.5:p.Val350Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1107G>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13281
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2150
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val370Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/1-168065807-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065807
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065807
    reference: chr 1
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1038G>T
  hgvsp: ENST00000367838.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.642G>T
  hgvsp: ENST00000367836.1:c.642G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1097G>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1038G>T
  hgvsp: ENST00000271357.5:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1038G>T
  hgvsp: ENST00000361697.2:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1038G>T
  hgvsp: ENST00000367835.1:c.1038G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.696G>T
  hgvsp: ENST00000546300.1:c.696G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.804G>T
  hgvsp: ENST00000539777.1:c.804G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1098G>T
  hgvsp: ENST00000537209.1:c.1098G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10497
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8122
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg366Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

1-168065808-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065808
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065808
    reference: chr 1
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.803G>A
  hgvsp: ENSP00000437576.1:p.Arg268Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1096G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1037G>A
  hgvsp: ENSP00000271357.5:p.Arg346Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1037G>A
  hgvsp: ENSP00000356809.1:p.Arg346Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1037G>A
  hgvsp: ENSP00000355194.2:p.Arg346Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.695G>A
  hgvsp: ENSP00000444348.1:p.Arg232Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1097G>A
  hgvsp: ENSP00000441039.1:p.Arg366Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.641G>A
  hgvsp: ENSP00000356810.1:p.Arg214Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1037G>A
  hgvsp: ENSP00000356812.1:p.Arg346Gln
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg366Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

1-168065809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065809
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065809
    reference: chr 1
allele count: 4
allele frequency: 3.296413502109704e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.694C>T
  hgvsp: ENSP00000444348.1:p.Arg232Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1036C>T
  hgvsp: ENSP00000356812.1:p.Arg346Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.640C>T
  hgvsp: ENSP00000356810.1:p.Arg214Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.802C>T
  hgvsp: ENSP00000437576.1:p.Arg268Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1036C>T
  hgvsp: ENSP00000271357.5:p.Arg346Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1036C>T
  hgvsp: ENSP00000356809.1:p.Arg346Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1036C>T
  hgvsp: ENSP00000355194.2:p.Arg346Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1096C>T
  hgvsp: ENSP00000441039.1:p.Arg366Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1095C>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8104
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21168
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg366Trp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

1-168065818-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065818
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065818
    reference: chr 1
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.685C>T
  hgvsp: ENSP00000444348.1:p.Arg229Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1027C>T
  hgvsp: ENSP00000356809.1:p.Arg343Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1027C>T
  hgvsp: ENSP00000356812.1:p.Arg343Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1027C>T
  hgvsp: ENSP00000355194.2:p.Arg343Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.793C>T
  hgvsp: ENSP00000437576.1:p.Arg265Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1086C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1087C>T
  hgvsp: ENSP00000441039.1:p.Arg363Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1027C>T
  hgvsp: ENSP00000271357.5:p.Arg343Trp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.631C>T
  hgvsp: ENSP00000356810.1:p.Arg211Trp
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4902
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg363Trp
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: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

1-168065818-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065818
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065818
    reference: chr 1
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.685C>A
  hgvsp: ENST00000546300.1:c.685C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1027C>A
  hgvsp: ENST00000271357.5:c.1027C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1087C>A
  hgvsp: ENST00000537209.1:c.1087C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1086C>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1027C>A
  hgvsp: ENST00000367835.1:c.1027C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1027C>A
  hgvsp: ENST00000367838.1:c.1027C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1027C>A
  hgvsp: ENST00000361697.2:c.1027C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.793C>A
  hgvsp: ENST00000539777.1:c.793C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.631C>A
  hgvsp: ENST00000367836.1:c.631C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12560
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21202
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3999
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg363Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/1-168065825-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065825
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065825
    reference: chr 1
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1020T>G
  hgvsp: ENSP00000271357.5:p.Phe340Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1020T>G
  hgvsp: ENSP00000355194.2:p.Phe340Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.678T>G
  hgvsp: ENSP00000444348.1:p.Phe226Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.786T>G
  hgvsp: ENSP00000437576.1:p.Phe262Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1020T>G
  hgvsp: ENSP00000356809.1:p.Phe340Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.624T>G
  hgvsp: ENSP00000356810.1:p.Phe208Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1079T>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1080T>G
  hgvsp: ENSP00000441039.1:p.Phe360Leu
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1020T>G
  hgvsp: ENSP00000356812.1:p.Phe340Leu
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe360Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

1-168065828-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065828
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065828
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1017C>T
  hgvsp: ENST00000361697.2:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1017C>T
  hgvsp: ENST00000271357.5:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1076C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1017C>T
  hgvsp: ENST00000367838.1:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.783C>T
  hgvsp: ENST00000539777.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1077C>T
  hgvsp: ENST00000537209.1:c.1077C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.675C>T
  hgvsp: ENST00000546300.1:c.675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1017C>T
  hgvsp: ENST00000367835.1:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.621C>T
  hgvsp: ENST00000367836.1:c.621C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12568
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21212
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4061
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys359Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

1-168065832-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065832
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065832
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1072T>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.617T>C
  hgvsp: ENSP00000356810.1:p.Met206Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.779T>C
  hgvsp: ENSP00000437576.1:p.Met260Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1013T>C
  hgvsp: ENSP00000271357.5:p.Met338Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1013T>C
  hgvsp: ENSP00000356809.1:p.Met338Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1013T>C
  hgvsp: ENSP00000356812.1:p.Met338Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1013T>C
  hgvsp: ENSP00000355194.2:p.Met338Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1073T>C
  hgvsp: ENSP00000441039.1:p.Met358Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.671T>C
  hgvsp: ENSP00000444348.1:p.Met224Thr
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4910
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met358Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

1-168065833-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065833
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065833
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.670A>G
  hgvsp: ENSP00000444348.1:p.Met224Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1012A>G
  hgvsp: ENSP00000356812.1:p.Met338Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1071A>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.616A>G
  hgvsp: ENSP00000356810.1:p.Met206Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1012A>G
  hgvsp: ENSP00000356809.1:p.Met338Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1072A>G
  hgvsp: ENSP00000441039.1:p.Met358Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1012A>G
  hgvsp: ENSP00000271357.5:p.Met338Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.778A>G
  hgvsp: ENSP00000437576.1:p.Met260Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1012A>G
  hgvsp: ENSP00000355194.2:p.Met338Val
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8107
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4000
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4907
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met358Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-168065834-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065834
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065834
    reference: chr 1
allele count: 5
allele frequency: 4.11868399808893e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.1011C>T
  hgvsp: ENST00000271357.5:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.615C>T
  hgvsp: ENST00000367836.1:c.615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1071C>T
  hgvsp: ENST00000537209.1:c.1071C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.669C>T
  hgvsp: ENST00000546300.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.1011C>T
  hgvsp: ENST00000361697.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.1011C>T
  hgvsp: ENST00000367835.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.1011C>T
  hgvsp: ENST00000367838.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.777C>T
  hgvsp: ENST00000539777.1:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1070C>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12564
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8136
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly357Gly
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-168065849-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065849
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065849
    reference: chr 1
allele count: 3
allele frequency: 2.471128976458378e-5
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1056C>T
  hgvsp: ENST00000537209.1:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1055C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.762C>T
  hgvsp: ENST00000539777.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.996C>T
  hgvsp: ENST00000361697.2:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.996C>T
  hgvsp: ENST00000367835.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.996C>T
  hgvsp: ENST00000271357.5:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.996C>T
  hgvsp: ENST00000367838.1:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.600C>T
  hgvsp: ENST00000367836.1:c.600C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.654C>T
  hgvsp: ENST00000546300.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12563
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg352Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum

1-168065850-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065850
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065850
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.995G>A
  hgvsp: ENSP00000356809.1:p.Arg332His
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1054G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.995G>A
  hgvsp: ENSP00000355194.2:p.Arg332His
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.761G>A
  hgvsp: ENSP00000437576.1:p.Arg254His
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.653G>A
  hgvsp: ENSP00000444348.1:p.Arg218His
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.995G>A
  hgvsp: ENSP00000271357.5:p.Arg332His
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1055G>A
  hgvsp: ENSP00000441039.1:p.Arg352His
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.599G>A
  hgvsp: ENSP00000356810.1:p.Arg200His
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.995G>A
  hgvsp: ENSP00000356812.1:p.Arg332His
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13274
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg352His
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

1-168065851-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065851
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065851
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.994C>T
  hgvsp: ENSP00000271357.5:p.Arg332Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.994C>T
  hgvsp: ENSP00000355194.2:p.Arg332Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.994C>T
  hgvsp: ENSP00000356812.1:p.Arg332Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.598C>T
  hgvsp: ENSP00000356810.1:p.Arg200Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.994C>T
  hgvsp: ENSP00000356809.1:p.Arg332Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.760C>T
  hgvsp: ENSP00000437576.1:p.Arg254Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1054C>T
  hgvsp: ENSP00000441039.1:p.Arg352Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.652C>T
  hgvsp: ENSP00000444348.1:p.Arg218Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1053C>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg352Cys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ

1-168065864-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065864
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065864
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.585G>C
  hgvsp: ENSP00000356810.1:p.Trp195Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.981G>C
  hgvsp: ENSP00000356812.1:p.Trp327Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.981G>C
  hgvsp: ENSP00000271357.5:p.Trp327Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.981G>C
  hgvsp: ENSP00000355194.2:p.Trp327Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.639G>C
  hgvsp: ENSP00000444348.1:p.Trp213Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.981G>C
  hgvsp: ENSP00000356809.1:p.Trp327Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1041G>C
  hgvsp: ENSP00000441039.1:p.Trp347Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1040G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.747G>C
  hgvsp: ENSP00000437576.1:p.Trp249Cys
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13273
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3998
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp347Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

1-168065867-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065867
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065867
    reference: chr 1
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.582C>T
  hgvsp: ENST00000367836.1:c.582C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.978C>T
  hgvsp: ENST00000271357.5:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.978C>T
  hgvsp: ENST00000367838.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.978C>T
  hgvsp: ENST00000367835.1:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.744C>T
  hgvsp: ENST00000539777.1:c.744C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1037C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1038C>T
  hgvsp: ENST00000537209.1:c.1038C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.636C>T
  hgvsp: ENST00000546300.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.978C>T
  hgvsp: ENST00000361697.2:c.978C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8116
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu346Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

1-168065869-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065869
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065869
    reference: chr 1
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.976C>G
  hgvsp: ENSP00000356809.1:p.Leu326Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.634C>G
  hgvsp: ENSP00000444348.1:p.Leu212Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.976C>G
  hgvsp: ENSP00000356812.1:p.Leu326Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.976C>G
  hgvsp: ENSP00000271357.5:p.Leu326Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.580C>G
  hgvsp: ENSP00000356810.1:p.Leu194Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.742C>G
  hgvsp: ENSP00000437576.1:p.Leu248Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1035C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.976C>G
  hgvsp: ENSP00000355194.2:p.Leu326Val
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1036C>G
  hgvsp: ENSP00000441039.1:p.Leu346Val
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu346Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-168065884-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065884
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065884
    reference: chr 1
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.961C>T
  hgvsp: ENSP00000356809.1:p.Pro321Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.565C>T
  hgvsp: ENSP00000356810.1:p.Pro189Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.961C>T
  hgvsp: ENSP00000355194.2:p.Pro321Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.727C>T
  hgvsp: ENSP00000437576.1:p.Pro243Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.961C>T
  hgvsp: ENSP00000356812.1:p.Pro321Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.961C>T
  hgvsp: ENSP00000271357.5:p.Pro321Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.619C>T
  hgvsp: ENSP00000444348.1:p.Pro207Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1021C>T
  hgvsp: ENSP00000441039.1:p.Pro341Ser
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1020C>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4055
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro341Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

1-168065896-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065896
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065896
    reference: chr 1
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.949G>A
  hgvsp: ENSP00000356812.1:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.949G>A
  hgvsp: ENSP00000271357.5:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.715G>A
  hgvsp: ENSP00000437576.1:p.Ala239Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1008G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1009G>A
  hgvsp: ENSP00000441039.1:p.Ala337Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.607G>A
  hgvsp: ENSP00000444348.1:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.949G>A
  hgvsp: ENSP00000356809.1:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.553G>A
  hgvsp: ENSP00000356810.1:p.Ala185Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.949G>A
  hgvsp: ENSP00000355194.2:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12536
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3993
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4896
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala337Thr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

1-168065897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065897
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065897
    reference: chr 1
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.552C>T
  hgvsp: ENST00000367836.1:c.552C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.606C>T
  hgvsp: ENST00000546300.1:c.606C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.948C>T
  hgvsp: ENST00000367838.1:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.948C>T
  hgvsp: ENST00000367835.1:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.714C>T
  hgvsp: ENST00000539777.1:c.714C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.1008C>T
  hgvsp: ENST00000537209.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.948C>T
  hgvsp: ENST00000271357.5:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.948C>T
  hgvsp: ENST00000361697.2:c.948C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.1007C>T
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser336Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

1-168065915-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065915
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065915
    reference: chr 1
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.588A>T
  hgvsp: ENST00000546300.1:c.588A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.930A>T
  hgvsp: ENST00000367835.1:c.930A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.534A>T
  hgvsp: ENST00000367836.1:c.534A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.930A>T
  hgvsp: ENST00000367838.1:c.930A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.930A>T
  hgvsp: ENST00000271357.5:c.930A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.930A>T
  hgvsp: ENST00000361697.2:c.930A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.989A>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.696A>T
  hgvsp: ENST00000539777.1:c.696A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.990A>T
  hgvsp: ENST00000537209.1:c.990A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12519
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3988
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr330Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

1-168065920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065920
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065920
    reference: chr 1
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.925G>A
  hgvsp: ENSP00000356812.1:p.Ala309Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.691G>A
  hgvsp: ENSP00000437576.1:p.Ala231Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.583G>A
  hgvsp: ENSP00000444348.1:p.Ala195Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.925G>A
  hgvsp: ENSP00000356809.1:p.Ala309Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.985G>A
  hgvsp: ENSP00000441039.1:p.Ala329Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.925G>A
  hgvsp: ENSP00000355194.2:p.Ala309Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.529G>A
  hgvsp: ENSP00000356810.1:p.Ala177Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.925G>A
  hgvsp: ENSP00000271357.5:p.Ala309Thr
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.984G>A
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2034
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4885
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala329Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

1-168065927-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065927
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065927
    reference: chr 1
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.918G>C
  hgvsp: ENSP00000356809.1:p.Glu306Asp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.918G>C
  hgvsp: ENSP00000355194.2:p.Glu306Asp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.576G>C
  hgvsp: ENSP00000444348.1:p.Glu192Asp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.977G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.684G>C
  hgvsp: ENSP00000437576.1:p.Glu228Asp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.918G>C
  hgvsp: ENSP00000356812.1:p.Glu306Asp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.522G>C
  hgvsp: ENSP00000356810.1:p.Glu174Asp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.918G>C
  hgvsp: ENSP00000271357.5:p.Glu306Asp
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.978G>C
  hgvsp: ENSP00000441039.1:p.Glu326Asp
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu326Asp
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

1-168065929-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065929
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065929
    reference: chr 1
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.916G>C
  hgvsp: ENSP00000356809.1:p.Glu306Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.916G>C
  hgvsp: ENSP00000271357.5:p.Glu306Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.574G>C
  hgvsp: ENSP00000444348.1:p.Glu192Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.975G>C
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.520G>C
  hgvsp: ENSP00000356810.1:p.Glu174Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.682G>C
  hgvsp: ENSP00000437576.1:p.Glu228Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.976G>C
  hgvsp: ENSP00000441039.1:p.Glu326Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.916G>C
  hgvsp: ENSP00000355194.2:p.Glu306Gln
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.916G>C
  hgvsp: ENSP00000356812.1:p.Glu306Gln
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4877
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu326Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/1-168065931-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065931
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065931
    reference: chr 1
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.914T>G
  hgvsp: ENSP00000356809.1:p.Leu305Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.572T>G
  hgvsp: ENSP00000444348.1:p.Leu191Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.914T>G
  hgvsp: ENSP00000356812.1:p.Leu305Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.973T>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.914T>G
  hgvsp: ENSP00000271357.5:p.Leu305Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.680T>G
  hgvsp: ENSP00000437576.1:p.Leu227Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.914T>G
  hgvsp: ENSP00000355194.2:p.Leu305Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.974T>G
  hgvsp: ENSP00000441039.1:p.Leu325Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.518T>G
  hgvsp: ENSP00000356810.1:p.Leu173Arg
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu325Arg
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

1-168065934-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065934
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065934
    reference: chr 1
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.515G>A
  hgvsp: ENSP00000356810.1:p.Ser172Asn
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.569G>A
  hgvsp: ENSP00000444348.1:p.Ser190Asn
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.911G>A
  hgvsp: ENSP00000271357.5:p.Ser304Asn
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.911G>A
  hgvsp: ENSP00000355194.2:p.Ser304Asn
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.971G>A
  hgvsp: ENSP00000441039.1:p.Ser324Asn
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.911G>A
  hgvsp: ENSP00000356812.1:p.Ser304Asn
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.970G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.911G>A
  hgvsp: ENSP00000356809.1:p.Ser304Asn
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.677G>A
  hgvsp: ENSP00000437576.1:p.Ser226Asn
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15635
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4870
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2147
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4028
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser324Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

1-168065940-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065940
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065940
    reference: chr 1
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.905C>T
  hgvsp: ENSP00000355194.2:p.Ser302Phe
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.905C>T
  hgvsp: ENSP00000356812.1:p.Ser302Phe
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.905C>T
  hgvsp: ENSP00000356809.1:p.Ser302Phe
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.905C>T
  hgvsp: ENSP00000271357.5:p.Ser302Phe
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.509C>T
  hgvsp: ENSP00000356810.1:p.Ser170Phe
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.563C>T
  hgvsp: ENSP00000444348.1:p.Ser188Phe
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.671C>T
  hgvsp: ENSP00000437576.1:p.Ser224Phe
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.964C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.965C>T
  hgvsp: ENSP00000441039.1:p.Ser322Phe
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser322Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

1-168065940-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065940
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065940
    reference: chr 1
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.964C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.965C>G
  hgvsp: ENSP00000441039.1:p.Ser322Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.671C>G
  hgvsp: ENSP00000437576.1:p.Ser224Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.905C>G
  hgvsp: ENSP00000355194.2:p.Ser302Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.905C>G
  hgvsp: ENSP00000356809.1:p.Ser302Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.563C>G
  hgvsp: ENSP00000444348.1:p.Ser188Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.905C>G
  hgvsp: ENSP00000271357.5:p.Ser302Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.509C>G
  hgvsp: ENSP00000356810.1:p.Ser170Cys
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.905C>G
  hgvsp: ENSP00000356812.1:p.Ser302Cys
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser322Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-168065942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065942
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065942
    reference: chr 1
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.903C>T
  hgvsp: ENST00000367835.1:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.669C>T
  hgvsp: ENST00000539777.1:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.561C>T
  hgvsp: ENST00000546300.1:c.561C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.507C>T
  hgvsp: ENST00000367836.1:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.903C>T
  hgvsp: ENST00000271357.5:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.903C>T
  hgvsp: ENST00000361697.2:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.903C>T
  hgvsp: ENST00000367838.1:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.962C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.963C>T
  hgvsp: ENST00000537209.1:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3975
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4872
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val321Val
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

1-168065944-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065944
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065944
    reference: chr 1
allele count: 7
allele frequency: 5.772434153018983e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.901G>A
  hgvsp: ENSP00000355194.2:p.Val301Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.901G>A
  hgvsp: ENSP00000271357.5:p.Val301Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.559G>A
  hgvsp: ENSP00000444348.1:p.Val187Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.961G>A
  hgvsp: ENSP00000441039.1:p.Val321Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.505G>A
  hgvsp: ENSP00000356810.1:p.Val169Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.667G>A
  hgvsp: ENSP00000437576.1:p.Val223Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.901G>A
  hgvsp: ENSP00000356809.1:p.Val301Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.960G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.901G>A
  hgvsp: ENSP00000356812.1:p.Val301Ile
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15676
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12453
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2907
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13270
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val321Ile
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

1-168065945-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065945
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065945
    reference: chr 1
allele count: 7
allele frequency: 5.771672630728385e-5
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.900C>T
  hgvsp: ENST00000361697.2:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.900C>T
  hgvsp: ENST00000367835.1:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.959C>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.960C>T
  hgvsp: ENST00000537209.1:c.960C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.504C>T
  hgvsp: ENST00000367836.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.666C>T
  hgvsp: ENST00000539777.1:c.666C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.900C>T
  hgvsp: ENST00000367838.1:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.900C>T
  hgvsp: ENST00000271357.5:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.558C>T
  hgvsp: ENST00000546300.1:c.558C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20599
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser320Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS

1-168065945-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065945
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065945
    reference: chr 1
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.900C>G
  hgvsp: ENST00000367835.1:c.900C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.960C>G
  hgvsp: ENST00000537209.1:c.960C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.558C>G
  hgvsp: ENST00000546300.1:c.558C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.900C>G
  hgvsp: ENST00000271357.5:c.900C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.504C>G
  hgvsp: ENST00000367836.1:c.504C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.959C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.666C>G
  hgvsp: ENST00000539777.1:c.666C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.900C>G
  hgvsp: ENST00000361697.2:c.900C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.900C>G
  hgvsp: ENST00000367838.1:c.900C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser320Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

1-168065948-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065948
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065948
    reference: chr 1
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.897C>G
  hgvsp: ENSP00000356812.1:p.Ser299Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.555C>G
  hgvsp: ENSP00000444348.1:p.Ser185Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.501C>G
  hgvsp: ENSP00000356810.1:p.Ser167Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.957C>G
  hgvsp: ENSP00000441039.1:p.Ser319Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.663C>G
  hgvsp: ENSP00000437576.1:p.Ser221Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.897C>G
  hgvsp: ENSP00000271357.5:p.Ser299Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.897C>G
  hgvsp: ENSP00000356809.1:p.Ser299Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.897C>G
  hgvsp: ENSP00000355194.2:p.Ser299Arg
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.956C>G
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5294
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12436
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser319Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/1-168065949-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065949
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065949
    reference: chr 1
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.896G>T
  hgvsp: ENSP00000271357.5:p.Ser299Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.896G>T
  hgvsp: ENSP00000355194.2:p.Ser299Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.896G>T
  hgvsp: ENSP00000356812.1:p.Ser299Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.662G>T
  hgvsp: ENSP00000437576.1:p.Ser221Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.956G>T
  hgvsp: ENSP00000441039.1:p.Ser319Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.896G>T
  hgvsp: ENSP00000356809.1:p.Ser299Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.500G>T
  hgvsp: ENSP00000356810.1:p.Ser167Ile
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.955G>T
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.554G>T
  hgvsp: ENSP00000444348.1:p.Ser185Ile
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15682
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3973
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser319Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

1-168065954-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065954
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065954
    reference: chr 1
allele count: 1
allele frequency: 8.247694769311978e-6
allele num: 121246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.657G>A
  hgvsp: ENST00000539777.1:c.657G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.891G>A
  hgvsp: ENST00000367838.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.549G>A
  hgvsp: ENST00000546300.1:c.549G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.495G>A
  hgvsp: ENST00000367836.1:c.495G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.951G>A
  hgvsp: ENST00000537209.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.891G>A
  hgvsp: ENST00000367835.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.950G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.891G>A
  hgvsp: ENST00000361697.2:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.891G>A
  hgvsp: ENST00000271357.5:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12441
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8016
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly317Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

1-168065960-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065960
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065960
    reference: chr 1
allele count: 2
allele frequency: 1.649402916144356e-5
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.489C>G
  hgvsp: ENST00000367836.1:c.489C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.885C>G
  hgvsp: ENST00000271357.5:c.885C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.944C>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.885C>G
  hgvsp: ENST00000361697.2:c.885C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.885C>G
  hgvsp: ENST00000367838.1:c.885C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.543C>G
  hgvsp: ENST00000546300.1:c.543C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.885C>G
  hgvsp: ENST00000367835.1:c.885C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.945C>G
  hgvsp: ENST00000537209.1:c.945C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.651C>G
  hgvsp: ENST00000539777.1:c.651C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7934
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13255
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Leu315Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

1-168065966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065966
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065966
    reference: chr 1
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.879G>A
  hgvsp: ENST00000361697.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.879G>A
  hgvsp: ENST00000367835.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.879G>A
  hgvsp: ENST00000271357.5:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.938G>A
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.645G>A
  hgvsp: ENST00000539777.1:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.537G>A
  hgvsp: ENST00000546300.1:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.939G>A
  hgvsp: ENST00000537209.1:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.879G>A
  hgvsp: ENST00000367838.1:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.483G>A
  hgvsp: ENST00000367836.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2031
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7934
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4002
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu313Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/1-168065969-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168065969
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 168065969
    reference: chr 1
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356810
  ensembl transcript: ENST00000367836
  gene symbol: GPR161
  hgvsc: ENST00000367836.1:c.480T>G
  hgvsp: ENST00000367836.1:c.480T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356812
  ensembl transcript: ENST00000367838
  gene symbol: GPR161
  hgvsc: ENST00000367838.1:c.876T>G
  hgvsp: ENST00000367838.1:c.876T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000441039
  ensembl transcript: ENST00000537209
  gene symbol: GPR161
  hgvsc: ENST00000537209.1:c.936T>G
  hgvsp: ENST00000537209.1:c.936T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000271357
  ensembl transcript: ENST00000271357
  gene symbol: GPR161
  hgvsc: ENST00000271357.5:c.876T>G
  hgvsp: ENST00000271357.5:c.876T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000444348
  ensembl transcript: ENST00000546300
  gene symbol: GPR161
  hgvsc: ENST00000546300.1:c.534T>G
  hgvsp: ENST00000546300.1:c.534T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000437576
  ensembl transcript: ENST00000539777
  gene symbol: GPR161
  hgvsc: ENST00000539777.1:c.642T>G
  hgvsp: ENST00000539777.1:c.642T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000356809
  ensembl transcript: ENST00000367835
  gene symbol: GPR161
  hgvsc: ENST00000367835.1:c.876T>G
  hgvsp: ENST00000367835.1:c.876T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000143147
  ensembl transcript: ENST00000493800
  gene symbol: GPR161
  hgvsc: ENST00000493800.1:n.935T>G
  variant of: http://identifiers.org/hgnc/23694
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000143147
  ensembl protein: ENSP00000355194
  ensembl transcript: ENST00000361697
  gene symbol: GPR161
  hgvsc: ENST00000361697.2:c.876T>G
  hgvsp: ENST00000361697.2:c.876T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23694
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser312Ser
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 1808
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2491
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2377
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 222
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 31902
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2095
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4126
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.125365743866757e-4
allele num: 8886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.106859365611461e-4
allele num: 63242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10938
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.24e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.42e0

QD
type: SiteQuality
SIO_000300: 2.967e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.361192e6

GenotypeQuality
all individuals: 1421
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30980
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4008
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1139
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3373
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2261
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15660
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.475845097785262e-5
allele num: 61768
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.219809709685289e-4
allele num: 8198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.453582907922102e-5
allele num: 10578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 5.52689756816507e-4
allele num: 5428
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.313e1

FS
type: SiteQuality
SIO_000300: 5.8729e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.586e0

DP
type: SiteQuality
SIO_000300: 1.367411e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.754e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.81e-1

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

GenotypeQuality
all individuals: 2672
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5972
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 857
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.299609424215698e-5
allele num: 15874
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64590
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
SIO_000300: 5.874e1

QD
type: SiteQuality
SIO_000300: 1.262e1

FS
type: SiteQuality
SIO_000300: 8.308e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

DP
type: SiteQuality
SIO_000300: 1.480028e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

GenotypeQuality
all individuals: 5972
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33574
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2672
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1612
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548227279764669e-5
allele num: 64590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11288
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

DP
type: SiteQuality
SIO_000300: 1.480028e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

QD
type: SiteQuality
SIO_000300: 1.262e1

MQ
type: SiteQuality
SIO_000300: 5.874e1

FS
type: SiteQuality
SIO_000300: 8.308e0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

GenotypeQuality
all individuals: 1722
bin: 2.25e1
variant carriers: 72

GenotypeQuality
all individuals: 870
bin: 7.25e1
variant carriers: 47

GenotypeQuality
all individuals: 1360
bin: 3.25e1
variant carriers: 48

GenotypeQuality
all individuals: 643
bin: 7.5e0
variant carriers: 77

GenotypeQuality
all individuals: 1654
bin: 5.75e1
variant carriers: 60

GenotypeQuality
all individuals: 735
bin: 8.25e1
variant carriers: 51

GenotypeQuality
all individuals: 901
bin: 1.75e1
variant carriers: 61

GenotypeQuality
all individuals: 1589
bin: 4.25e1
variant carriers: 66

GenotypeQuality
all individuals: 804
bin: 7.75e1
variant carriers: 57

GenotypeQuality
all individuals: 1640
bin: 4.75e1
variant carriers: 71

GenotypeQuality
all individuals: 667
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variant carriers: 49

GenotypeQuality
all individuals: 616
bin: 9.25e1
variant carriers: 51

GenotypeQuality
all individuals: 1515
bin: 3.75e1
variant carriers: 69

GenotypeQuality
all individuals: 20927
bin: 9.75e1
variant carriers: 1103

GenotypeQuality
all individuals: 1157
bin: 2.75e1
variant carriers: 69

GenotypeQuality
all individuals: 15993
bin: 6.25e1
variant carriers: 64

South Asian
type: Population
allele count: 55
allele frequency: 3.605138961719979e-3
allele num: 15256
num of homozygotes: 0

East Asian
type: Population
allele count: 178
allele frequency: 2.306296968126458e-2
allele num: 7718
num of homozygotes: 0

African
type: Population
allele count: 195
allele frequency: 2.265861027190332e-2
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1158
allele frequency: 1.980096439930235e-2
allele num: 58482
num of homozygotes: 0

Other
type: Population
allele count: 19
allele frequency: 2.448453608247423e-2
allele num: 776
num of homozygotes: 0

Latino
type: Population
allele count: 171
allele frequency: 1.68506109578242e-2
allele num: 10148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 215
allele frequency: 4.035285285285285e-2
allele num: 5328
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.28e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.162e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

QD
type: SiteQuality
SIO_000300: 1.041e1

FS
type: SiteQuality
SIO_000300: 8.381e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

DP
type: SiteQuality
SIO_000300: 1.637335e6

GenotypeQuality
all individuals: 804
bin: 7.75e1
variant carriers: 627

GenotypeQuality
all individuals: 1589
bin: 4.25e1
variant carriers: 1024

GenotypeQuality
all individuals: 643
bin: 7.5e0
variant carriers: 288

GenotypeQuality
all individuals: 664
bin: 1.25e1
variant carriers: 333

GenotypeQuality
all individuals: 1157
bin: 2.75e1
variant carriers: 694

GenotypeQuality
all individuals: 20927
bin: 9.75e1
variant carriers: 19845

GenotypeQuality
all individuals: 1722
bin: 2.25e1
variant carriers: 663

GenotypeQuality
all individuals: 1643
bin: 6.75e1
variant carriers: 744

GenotypeQuality
all individuals: 901
bin: 1.75e1
variant carriers: 465

GenotypeQuality
all individuals: 870
bin: 7.25e1
variant carriers: 670

GenotypeQuality
all individuals: 735
bin: 8.25e1
variant carriers: 635

GenotypeQuality
all individuals: 1515
bin: 3.75e1
variant carriers: 980

GenotypeQuality
all individuals: 15993
bin: 6.25e1
variant carriers: 811

GenotypeQuality
all individuals: 1704
bin: 5.25e1
variant carriers: 911

GenotypeQuality
all individuals: 1654
bin: 5.75e1
variant carriers: 847

GenotypeQuality
all individuals: 616
bin: 9.25e1
variant carriers: 540

European (Non-Finnish)
type: Population
allele count: 19405
allele frequency: 3.318114975548032e-1
allele num: 58482
num of homozygotes: 3134

European (Finnish)
type: Population
allele count: 1925
allele frequency: 3.612987987987988e-1
allele num: 5328
num of homozygotes: 332

East Asian
type: Population
allele count: 1557
allele frequency: 2.017362010883649e-1
allele num: 7718
num of homozygotes: 131

African
type: Population
allele count: 5315
allele frequency: 6.175923774111085e-1
allele num: 8606
num of homozygotes: 1649

Latino
type: Population
allele count: 5542
allele frequency: 5.46117461568782e-1
allele num: 10148
num of homozygotes: 1481

Other
type: Population
allele count: 268
allele frequency: 3.45360824742268e-1
allele num: 776
num of homozygotes: 51

South Asian
type: Population
allele count: 3616
allele frequency: 2.370214997378081e-1
allele num: 15256
num of homozygotes: 461

MQ
type: SiteQuality
SIO_000300: 5.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.162e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.6e-2

FS
type: SiteQuality
SIO_000300: 8.381e0

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.28e-1

DP
type: SiteQuality
SIO_000300: 1.637335e6

QD
type: SiteQuality
SIO_000300: 1.041e1

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
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variant carriers: 0

GenotypeQuality
all individuals: 5481
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variant carriers: 0

GenotypeQuality
all individuals: 424
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variant carriers: 0

GenotypeQuality
all individuals: 189
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variant carriers: 0

GenotypeQuality
all individuals: 431
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variant carriers: 0

GenotypeQuality
all individuals: 568
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variant carriers: 0

GenotypeQuality
all individuals: 112
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GenotypeQuality
all individuals: 322
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variant carriers: 3

GenotypeQuality
all individuals: 544
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
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variant carriers: 0

GenotypeQuality
all individuals: 45500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15716
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11248
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.630487127245786e-5
allele num: 64788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.876e1

VQSLOD
type: SiteQuality
SIO_000300: -1.683e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.015e0

DP
type: SiteQuality
SIO_000300: 1.488849e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.39e-1

FS
type: SiteQuality
SIO_000300: 1.346e0

MQRankSum
type: SiteQuality
SIO_000300: -1.363e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.13e1

GenotypeQuality
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 5140
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 401
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45508
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.368647100930566e-4
allele num: 11176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64362
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

MQ
type: SiteQuality
SIO_000300: 5.869e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.504e0

DP
type: SiteQuality
SIO_000300: 1.473234e6

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 521
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45166
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1043
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.320185614849188e-3
allele num: 862
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.283288465520812e-4
allele num: 9658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55714730613516e-5
allele num: 64220
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.862428348097968e-4
allele num: 15352
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.968e0

QD
type: SiteQuality
SIO_000300: 1.266e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

MQ
type: SiteQuality
SIO_000300: 5.886e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

DP
type: SiteQuality
SIO_000300: 1.46852e6

GenotypeQuality
all individuals: 161
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4321
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
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GenotypeQuality
all individuals: 509
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5074
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GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
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GenotypeQuality
all individuals: 588
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 110
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64160
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.531678641410843e-5
allele num: 15310
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

MQ
type: SiteQuality
SIO_000300: 5.922e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.433e0

FS
type: SiteQuality
SIO_000300: 4.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.464166e6

QD
type: SiteQuality
SIO_000300: 1.164e1

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1003
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5016
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
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GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
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GenotypeQuality
all individuals: 4754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1043
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45000
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.009009009009009e-5
allele num: 11100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.127541127165822e-5
allele num: 63948
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e0

MQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.701e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.15e-1

QD
type: SiteQuality
SIO_000300: 1.843e1

DP
type: SiteQuality
SIO_000300: 1.456612e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.339e0

FS
type: SiteQuality
SIO_000300: 1.932e0

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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bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57848213158227e-5
allele num: 63352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8418
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

DP
type: SiteQuality
SIO_000300: 1.436353e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.763e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 4.264e0

QD
type: SiteQuality
SIO_000300: 1.308e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.66e-1

MQ
type: SiteQuality
SIO_000300: 5.904e1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10956
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63120
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.750371270419872e-5
allele num: 14814
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: -1.243e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.068e1

MQRankSum
type: SiteQuality
SIO_000300: 7.74e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

FS
type: SiteQuality
SIO_000300: 1.83e0

VQSLOD
type: SiteQuality
SIO_000300: -2.245e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.035e0

DP
type: SiteQuality
SIO_000300: 1.428278e6

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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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8370
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.362954886193267e-4
allele num: 14674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62820
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.89e-1

FS
type: SiteQuality
SIO_000300: 3.117e0

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

DP
type: SiteQuality
SIO_000300: 1.417054e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.503e0

QD
type: SiteQuality
SIO_000300: 1.059e1

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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bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.184834123222749e-3
allele num: 844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.87e1

VQSLOD
type: SiteQuality
SIO_000300: -2.104e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

FS
type: SiteQuality
SIO_000300: 4.871e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

DP
type: SiteQuality
SIO_000300: 1.411568e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.393e0

QD
type: SiteQuality
SIO_000300: 4.83e0

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: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.720045409198803e-5
allele num: 58138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.750999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -9.897e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.728e1

MQRankSum
type: SiteQuality
SIO_000300: -8.33e-1

DP
type: SiteQuality
SIO_000300: 1.214681e6

QD
type: SiteQuality
SIO_000300: 1.645e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7000
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.600985773496135e-5
allele num: 53562
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9010
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

ClippingRankSum
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SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.8276e5

QD
type: SiteQuality
SIO_000300: 1.38e1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48514
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.011122345803842e-4
allele num: 9890
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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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5174
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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FS
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BaseQRankSum
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SIO_000300: -1.67e0

MQRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

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

African
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allele 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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9570
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.114343707713126e-5
allele num: 47296
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: 8.25e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.566e1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 7468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 8.817953353026762e-5
allele num: 45362
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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.196e0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.13e-2

FS
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.117e1

DP
type: SiteQuality
SIO_000300: 7.35398e5

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7344
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4244
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4792
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.643655489809336e-4
allele num: 6084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

DP
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SIO_000300: 6.74555e5

ClippingRankSum
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SIO_000300: 1.2e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.74e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.001e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64450
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.334267040149393e-4
allele num: 8568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
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: 814
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.491e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e0

FS
type: SiteQuality
SIO_000300: 2.015e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.516e0

VQSLOD
type: SiteQuality
SIO_000300: 1.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.933191e6

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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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64522
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: 1
allele frequency: 9.809691975671964e-5
allele num: 10194
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
allele num: 8576
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.945707e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.136e0

QD
type: SiteQuality
SIO_000300: 1.509e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.45e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547939692269589e-5
allele num: 64602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
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: 1
allele frequency: 9.784735812133073e-5
allele num: 10220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10574
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 6.989748369058714e-4
allele num: 8584
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 1.241e0

QD
type: SiteQuality
SIO_000300: 1.187e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.953903e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

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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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
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: 834
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.344803614876608e-4
allele num: 11508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64768
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.257e1

FS
type: SiteQuality
SIO_000300: 9.69e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
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DP
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10334
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.450454865684443e-4
allele num: 65294
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.173708920187793e-3
allele num: 852
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South Asian
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allele count: 26
allele frequency: 2.089360334297654e-3
allele num: 12444
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.56e-1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.96e0

DP
type: SiteQuality
SIO_000300: 1.984419e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 852
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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allele frequency: 8.671522719389525e-4
allele num: 11532
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African
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65294
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East Asian
type: Population
allele count: 0
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MQ
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.56e-1

DP
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QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
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: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
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South Asian
type: Population
allele count: 0
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East Asian
type: Population
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allele num: 8632
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African
type: Population
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FS
type: SiteQuality
SIO_000300: 3.866e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.57e-1

QD
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SIO_000300: 1.236e1

ClippingRankSum
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SIO_000300: -7.0e-1

DP
type: SiteQuality
SIO_000300: 1.98901e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.01e-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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bin: 9.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13020
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.526158354190831e-5
allele num: 65524
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.028e1

VQSLOD
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FS
type: SiteQuality
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QD
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DP
type: SiteQuality
SIO_000300: 1.990636e6

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.26e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.13e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66006
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.885155604516663e-5
allele num: 14524
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503171692270691e-5
allele num: 66526
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.79e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.676e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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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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variant carriers: 2

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

South Asian
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allele count: 2
allele frequency: 1.228803145736053e-4
allele num: 16276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 2.039362e6

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.4e-2

FS
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SIO_000300: 1.416e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

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

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

South Asian
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allele count: 0
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ClippingRankSum
type: SiteQuality
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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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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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66696
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.949e1

FS
type: SiteQuality
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InbreedingCoeff
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ClippingRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele num: 66696
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South Asian
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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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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variant carriers: 0

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 66704
num of homozygotes: 0

European (Finnish)
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allele num: 6614
num of homozygotes: 0

African
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South Asian
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Latino
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Other
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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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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bin: 2.25e1
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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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bin: 6.75e1
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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

GenotypeQuality
all individuals: 13280
bin: 9.75e1
variant carriers: 3

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212268153715602e-4
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 2.043546e6

FS
type: SiteQuality
SIO_000300: 2.482e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 3.39e0

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

QD
type: SiteQuality
SIO_000300: 1.081e1

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: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.482e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: 6.24e-1

DP
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SIO_000300: 2.043546e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.081e1

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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bin: 3.25e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.443e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.739e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

InbreedingCoeff
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MQRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 2.251e0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 2.043671e6

MQ
type: SiteQuality
SIO_000300: 5.957e1

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: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.379e1

MQ
type: SiteQuality
SIO_000300: 5.989e1

FS
type: SiteQuality
SIO_000300: 2.037e0

MQRankSum
type: SiteQuality
SIO_000300: 7.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.081e0

DP
type: SiteQuality
SIO_000300: 2.043726e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.265e0

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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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.447e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.94e-1

DP
type: SiteQuality
SIO_000300: 2.043635e6

InbreedingCoeff
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SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

FS
type: SiteQuality
SIO_000300: 7.164e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

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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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 1
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allele num: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.963e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

DP
type: SiteQuality
SIO_000300: 2.043675e6

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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variant carriers: 0

Latino
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allele count: 5
allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.29e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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MQ
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-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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variant carriers: 0

South Asian
type: Population
allele count: 0
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
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

European (Finnish)
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allele frequency: 0.0e0
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African
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East Asian
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allele num: 8652
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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QD
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DP
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VQSLOD
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MQ
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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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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African
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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South Asian
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Other
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African
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Latino
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South Asian
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VQSLOD
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MQ
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MQRankSum
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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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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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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South Asian
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DP
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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InbreedingCoeff
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MQ
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VQSLOD
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BaseQRankSum
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QD
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FS
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DP
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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African
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European (Non-Finnish)
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East Asian
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European (Finnish)
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InbreedingCoeff
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQ
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QD
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ClippingRankSum
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GenotypeQuality
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South Asian
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African
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East Asian
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQ
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FS
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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Latino
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African
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Other
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South Asian
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European (Finnish)
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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QD
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele num: 66680
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Latino
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Other
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European (Finnish)
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MQ
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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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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Other
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East Asian
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African
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Latino
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allele num: 11578
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European (Finnish)
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European (Non-Finnish)
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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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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European (Finnish)
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num of homozygotes: 0

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

Other
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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VQSLOD
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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Latino
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Other
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South Asian
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European (Finnish)
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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FS
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VQSLOD
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MQRankSum
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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Latino
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Other
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European (Non-Finnish)
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South Asian
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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South Asian
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FS
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ClippingRankSum
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MQRankSum
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QD
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.905e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.368e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.67e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

VQSLOD
type: SiteQuality
SIO_000300: 9.79e-1

DP
type: SiteQuality
SIO_000300: 2.03693e6

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.09e-1

GenotypeQuality
all individuals: 7
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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bin: 3.25e1
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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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variant carriers: 0

GenotypeQuality
all individuals: 95
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variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
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: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.003061040753856e-5
allele num: 66644
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.037163e6

MQRankSum
type: SiteQuality
SIO_000300: -5.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.91e-1

BaseQRankSum
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SIO_000300: 1.13e-1

InbreedingCoeff
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SIO_000300: 8.200000000000001e-3

VQSLOD
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SIO_000300: 1.14e0

ReadPosRankSum
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SIO_000300: -8.34e-1

FS
type: SiteQuality
SIO_000300: 5.28e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.211e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 7

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

African
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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: 8650
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.501875468867217e-5
allele num: 66650
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.413e1

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.67e-1

DP
type: SiteQuality
SIO_000300: 2.037012e6

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.16e-1

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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.037012e6

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.67e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 1.413e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e0

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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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.926782273603083e-4
allele num: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.408e0

DP
type: SiteQuality
SIO_000300: 2.036432e6

FS
type: SiteQuality
SIO_000300: 3.442e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

MQRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
type: SiteQuality
SIO_000300: 1.299e1

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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variant carriers: 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: 66642
num of homozygotes: 0

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

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

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

East Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: -5.434e0

FS
type: SiteQuality
SIO_000300: 5.366e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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VQSLOD
type: SiteQuality
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ClippingRankSum
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SIO_000300: -2.596e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
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SIO_000300: 2.31e0

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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South Asian
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allele count: 0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.94e-2

ReadPosRankSum
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BaseQRankSum
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DP
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FS
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MQRankSum
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MQ
type: SiteQuality
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QD
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
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num of homozygotes: 0

South Asian
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East Asian
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African
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Other
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European (Non-Finnish)
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ReadPosRankSum
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QD
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FS
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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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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European (Non-Finnish)
type: Population
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allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6614
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South Asian
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num of homozygotes: 0

Latino
type: Population
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Other
type: Population
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African
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East Asian
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
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FS
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QD
type: SiteQuality
SIO_000300: 1.429e1

VQSLOD
type: SiteQuality
SIO_000300: 8.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.035901e6