http://identifiers.org/exac.variant/7-126698163-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698163
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698163
    reference: chr 7
allele count: 1
allele frequency: 1.320166869092253e-5
allele num: 75748
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48387T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48387T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48387T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.76T>G
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48387T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48387T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47187T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48387T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48387T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48387T>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25177
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20297
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2209
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-126698165-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698165
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698165
    reference: chr 7
allele count: 25
allele frequency: 3.246753246753247e-4
allele num: 77000
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48385C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48385C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48385C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48385C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47185C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.74C>T
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48385C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48385C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48385C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48385C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25836
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4611
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 818
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19831
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/7-126698169-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698169
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698169
    reference: chr 7
allele count: 1
allele frequency: 1.268198650636636e-5
allele num: 78852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48381G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.70G>T
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48381G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48381G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48381G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48381G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48381G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48381G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47181G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48381G>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18952
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2210
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

7-126698169-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698169
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698169
    reference: chr 7
allele count: 1
allele frequency: 1.268198650636636e-5
allele num: 78852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48381G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48381G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48381G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48381G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48381G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48381G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47181G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.70G>A
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48381G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48381G>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
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: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-126698171-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698171
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698171
    reference: chr 7
allele count: 3
allele frequency: 3.753096304451172e-5
allele num: 79934
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47179A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.68A>G
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48379A>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26937
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

7-126698184-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698184
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698184
    reference: chr 7
allele count: 2
allele frequency: 2.36630383341221e-5
allele num: 84520
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48366T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48366T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48366T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48366T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48366T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48366T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47166T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.55T>A
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48366T>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48366T>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28795
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

7-126698186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698186
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698186
    reference: chr 7
allele count: 8
allele frequency: 9.40004230019035e-5
allele num: 85106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48364C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48364C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48364C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48364C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48364C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47164C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.53C>T
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48364C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48364C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48364C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

7-126698188-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698188
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698188
    reference: chr 7
allele count: 1
allele frequency: 1.168169711695715e-5
allele num: 85604
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.51A>G
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48362A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47162A>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16040
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29014
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16963
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

7-126698195-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698195
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698195
    reference: chr 7
allele count: 1
allele frequency: 1.174205063172232e-5
allele num: 85164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47155A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48355A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48355A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48355A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.44A>G
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48355A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48355A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48355A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48355A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48355A>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28533
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-126698204-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698204
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698204
    reference: chr 7
allele count: 1
allele frequency: 1.183684098387822e-5
allele num: 84482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48346T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48346T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48346T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48346T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48346T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.35T>G
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47146T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48346T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48346T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48346T>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: mature miRNA
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-126698214-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698214
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698214
    reference: chr 7
allele count: 1
allele frequency: 1.205022533921384e-5
allele num: 82986
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48336T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48336T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48336T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48336T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48336T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48336T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.25T>C
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47136T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48336T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48336T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: mature miRNA
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16782
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23859
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20080
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

7-126698215-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698215
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698215
    reference: chr 7
allele count: 1
allele frequency: 1.204674135646308e-5
allele num: 83010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48335A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: mature_miRNA_variant
  ensembl gene: ENSG00000207692
  ensembl transcript: ENST00000384959
  gene symbol: MIR592
  hgvsc: ENST00000384959.1:n.24A>T
  variant of: http://identifiers.org/hgnc/32848
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48335A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48335A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48335A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48335A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48335A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47135A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48335A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48335A>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: mature miRNA
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6257
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2334
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2128
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-126698255-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698255
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698255
    reference: chr 7
allele count: 1
allele frequency: 1.515564851019975e-5
allele num: 65982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48295T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48295T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48295T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48295T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48295T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47095T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48295T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48295T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48295T>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26908
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1554
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

7-126698259-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698259
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698259
    reference: chr 7
allele count: 1
allele frequency: 1.585389054473968e-5
allele num: 63076
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48291C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47091C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8870
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2855
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2206
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

7-126698261-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698261
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698261
    reference: chr 7
allele count: 1
allele frequency: 1.62871754780286e-5
allele num: 61398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48289T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48289T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48289T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47089T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48289T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48289T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48289T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48289T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48289T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19252
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

7-126698264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698264
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698264
    reference: chr 7
allele count: 1
allele frequency: 1.672240802675585e-5
allele num: 59800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48286G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48286G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48286G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48286G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48286G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47086G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48286G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48286G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48286G>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14837
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

7-126698273-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698273
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698273
    reference: chr 7
allele count: 33
allele frequency: 5.955818654345943e-4
allele num: 55408
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48277G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47077G>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 20410
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13282
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20940
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12778
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

7-126698276-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126698276
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126698277
    reference: chr 7
allele count: 1
allele frequency: 1.874414245548266e-5
allele num: 53350
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+48273dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+47073dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+48273dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+48273dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+48273dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+48273dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+48273dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+48273dupG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+48273dupG
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21034
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3271
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

7-126716149-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716149
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716149
    reference: chr 7
allele count: 2
allele frequency: 1.92975685063682e-4
allele num: 10364
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30401A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29201A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.*23A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30401A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30401A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30401A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30401A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30401A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30401A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30401A>C
  variant of: http://identifiers.org/hgnc/4600
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

7-126716170-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716170
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716170
    reference: chr 7
allele count: 1
allele frequency: 9.1441111923921e-5
allele num: 10936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.*2C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30380C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29180C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ

7-126716179-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716179
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716179
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 11116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30371T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29171T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30371T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30371T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30371T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.269T>C
  hgvsp: ENSP00000418255.1:p.Val90Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30371T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30371T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30371T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30371T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val90Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

7-126716194-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716194
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716194
    reference: chr 7
allele count: 1
allele frequency: 8.873114463176575e-5
allele num: 11270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30356C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30356C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30356C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30356C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29156C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30356C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30356C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.254C>G
  hgvsp: ENSP00000418255.1:p.Ser85Ter
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30356C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30356C>G
  variant of: http://identifiers.org/hgnc/4600
canonical: false
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser85Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-126716213-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716213
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716213
    reference: chr 7
allele count: 3
allele frequency: 2.631117347833714e-4
allele num: 11402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30337C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30337C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30337C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30337C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30337C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.235C>A
  hgvsp: ENSP00000418255.1:p.Leu79Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30337C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29137C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30337C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30337C>A
  variant of: http://identifiers.org/hgnc/4600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu79Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

7-126716276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716276
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716276
    reference: chr 7
allele count: 7
allele frequency: 6.136044880785414e-4
allele num: 11408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30274T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30274T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30274T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.172T>C
  hgvsp: ENSP00000418255.1:p.Phe58Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30274T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30274T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30274T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30274T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29074T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30274T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Phe58Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-126716302-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716302
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716303
    reference: chr 7
allele count: 5
allele frequency: 4.511820970943873e-4
allele num: 11082
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30247dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30247dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30247dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29047dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30247dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.158-13dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30247dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30247dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30247dupT
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30247dupT
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.5e0
  variant carriers: 1
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

7-126716303-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716303
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716303
    reference: chr 7
allele count: 1
allele frequency: 9.072763563781528e-5
allele num: 11022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30247T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29047T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.158-13T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30247T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30247T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30247T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30247T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30247T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30247T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30247T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

7-126716305-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716305
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716304
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 11070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.158-16delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30244delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30244delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30244delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30244delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30244delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30244delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30244delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29044delC
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30244delC
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3255
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: AG
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP

7-126716306-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716306
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716306
    reference: chr 7
allele count: 3741
allele frequency: 3.33779443254818e-1
allele num: 11208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30244C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30244C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30244C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30244C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29044C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30244C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.158-16C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30244C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30244C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30244C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.25e1
  variant carriers: 227
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.5e0
  variant carriers: 274
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 553
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 166
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.25e1
  variant carriers: 376
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.25e1
  variant carriers: 588
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 2.5e0
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.75e1
  variant carriers: 489
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 2.25e1
  variant carriers: 289
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 211
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.5e0
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 3.25e1
  variant carriers: 40
num of homozygotes: 677
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

7-126716311-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716311
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716311
    reference: chr 7
allele count: 1
allele frequency: 9.242144177449168e-5
allele num: 10820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30239T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30239T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29039T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30239T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30239T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30239T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30239T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.158-21T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30239T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30239T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/7-126716324-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126716324
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126716323
    reference: chr 7
allele count: 1
allele frequency: 9.46969696969697e-5
allele num: 10560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+30225delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+30225delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+30225delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.444+29025delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.158-35delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+30225delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+30225delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+30225delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+30225delG
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+30225delG
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: AC
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

7-126746500-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746500
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746500
    reference: chr 7
allele count: 1
allele frequency: 9.143275121148396e-6
allele num: 109370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.157+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.481+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.369+50A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+50A>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17161
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5349
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

7-126746503-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746503
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746503
    reference: chr 7
allele count: 4
allele frequency: 3.672487559448392e-5
allele num: 108918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.369+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.481+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+47C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.157+47C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15431
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16433
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6373
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

7-126746506-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746506
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746506
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 109692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.369+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.481+44T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.157+44T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

7-126746508-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746508
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746508
    reference: chr 7
allele count: 1
allele frequency: 9.120758847136081e-6
allele num: 109640
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.369+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.157+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+42G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.481+42G>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15982
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17002
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

7-126746512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746512
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746512
    reference: chr 7
allele count: 4
allele frequency: 3.636892638929299e-5
allele num: 109984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.481+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.369+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.157+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+38G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+38G>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-126746513-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746513
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746513
    reference: chr 7
allele count: 1
allele frequency: 9.058627436770781e-6
allele num: 110392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.369+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.481+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.157+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+37T>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+37T>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21887
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14428
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/7-126746517-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746517
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746517
    reference: chr 7
allele count: 2
allele frequency: 1.807076511619502e-5
allele num: 110676
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.727+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.369+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.481+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.727+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.727+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.727+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.727+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.727+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.157+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.269+33G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.727+33G>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2015
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12380
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5414
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

7-126746555-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746555
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746555
    reference: chr 7
allele count: 2
allele frequency: 1.667472611762352e-5
allele num: 119942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.152A>T
  hgvsp: ENSP00000418255.1:p.Glu51Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.722A>T
  hgvsp: ENSP00000351142.3:p.Glu241Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.264A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.364A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.722A>T
  hgvsp: ENSP00000415522.1:p.Glu241Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.722A>T
  hgvsp: ENSP00000409790.2:p.Glu241Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.722A>T
  hgvsp: ENSP00000345747.3:p.Glu241Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.722A>T
  hgvsp: ENSP00000385731.1:p.Glu241Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.722A>T
  hgvsp: ENSP00000419832.1:p.Glu241Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.722A>T
  hgvsp: ENSP00000344173.2:p.Glu241Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.476A>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu241Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

7-126746560-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746560
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746560
    reference: chr 7
allele count: 1
allele frequency: 8.305785810395521e-6
allele num: 120398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.259G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.717G>A
  hgvsp: ENST00000472701.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.717G>A
  hgvsp: ENST00000457830.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.359G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.717G>A
  hgvsp: ENST00000405249.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.717G>A
  hgvsp: ENST00000358373.3:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.147G>A
  hgvsp: ENST00000465844.1:c.147G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.717G>A
  hgvsp: ENST00000339582.2:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.717G>A
  hgvsp: ENST00000341617.3:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.471G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.717G>A
  hgvsp: ENST00000444921.2:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser239Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

7-126746561-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746561
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746561
    reference: chr 7
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.716C>T
  hgvsp: ENSP00000415522.1:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.716C>T
  hgvsp: ENSP00000419832.1:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.146C>T
  hgvsp: ENSP00000418255.1:p.Ser49Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.716C>T
  hgvsp: ENSP00000345747.3:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.716C>T
  hgvsp: ENSP00000344173.2:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.716C>T
  hgvsp: ENSP00000351142.3:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.716C>T
  hgvsp: ENSP00000385731.1:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.358C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.470C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.716C>T
  hgvsp: ENSP00000409790.2:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.258C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser239Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

7-126746561-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746561
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746561
    reference: chr 7
allele count: 1
allele frequency: 8.297102651754007e-6
allele num: 120524
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.716C>G
  hgvsp: ENSP00000415522.1:p.Ser239Trp
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.258C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.716C>G
  hgvsp: ENSP00000345747.3:p.Ser239Trp
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.716C>G
  hgvsp: ENSP00000409790.2:p.Ser239Trp
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.716C>G
  hgvsp: ENSP00000385731.1:p.Ser239Trp
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.470C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.146C>G
  hgvsp: ENSP00000418255.1:p.Ser49Trp
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.716C>G
  hgvsp: ENSP00000344173.2:p.Ser239Trp
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.716C>G
  hgvsp: ENSP00000419832.1:p.Ser239Trp
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.358C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.716C>G
  hgvsp: ENSP00000351142.3:p.Ser239Trp
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser239Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

7-126746569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746569
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746569
    reference: chr 7
allele count: 4
allele frequency: 3.311367926090268e-5
allele num: 120796
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.708C>T
  hgvsp: ENST00000339582.2:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.708C>T
  hgvsp: ENST00000457830.1:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.708C>T
  hgvsp: ENST00000472701.1:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.138C>T
  hgvsp: ENST00000465844.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.708C>T
  hgvsp: ENST00000444921.2:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.350C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.708C>T
  hgvsp: ENST00000405249.1:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.708C>T
  hgvsp: ENST00000341617.3:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.250C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.708C>T
  hgvsp: ENST00000358373.3:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.462C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41186
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12054
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr236Thr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

7-126746570-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746570
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746570
    reference: chr 7
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.137C>G
  hgvsp: ENSP00000418255.1:p.Thr46Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.461C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.707C>G
  hgvsp: ENSP00000385731.1:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.707C>G
  hgvsp: ENSP00000344173.2:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.707C>G
  hgvsp: ENSP00000351142.3:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.707C>G
  hgvsp: ENSP00000345747.3:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.249C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.349C>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.707C>G
  hgvsp: ENSP00000415522.1:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.707C>G
  hgvsp: ENSP00000419832.1:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.707C>G
  hgvsp: ENSP00000409790.2:p.Thr236Ser
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr236Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-126746583-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746583
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746583
    reference: chr 7
allele count: 1
allele frequency: 8.264599414866361e-6
allele num: 120998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.694G>A
  hgvsp: ENSP00000345747.3:p.Val232Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.694G>A
  hgvsp: ENSP00000385731.1:p.Val232Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.124G>A
  hgvsp: ENSP00000418255.1:p.Val42Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.694G>A
  hgvsp: ENSP00000419832.1:p.Val232Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.336G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.236G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.694G>A
  hgvsp: ENSP00000344173.2:p.Val232Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.694G>A
  hgvsp: ENSP00000409790.2:p.Val232Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.694G>A
  hgvsp: ENSP00000351142.3:p.Val232Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.448G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.694G>A
  hgvsp: ENSP00000415522.1:p.Val232Met
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val232Met
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

7-126746584-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746584
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746584
    reference: chr 7
allele count: 491
allele frequency: 4.057180631300611e-3
allele num: 121020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.447T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.693T>C
  hgvsp: ENST00000339582.2:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.235T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.693T>C
  hgvsp: ENST00000341617.3:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.693T>C
  hgvsp: ENST00000405249.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.693T>C
  hgvsp: ENST00000358373.3:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.335T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.123T>C
  hgvsp: ENST00000465844.1:c.123T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.693T>C
  hgvsp: ENST00000457830.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.693T>C
  hgvsp: ENST00000472701.1:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.693T>C
  hgvsp: ENST00000444921.2:c.693T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12370
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 5.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 40613
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3208
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.75e1
  variant carriers: 30
genotype quality: GenotypeQuality
hgvs: p.Gly231Gly
num of homozygotes: 14
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

7-126746587-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746587
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746587
    reference: chr 7
allele count: 3
allele frequency: 2.478355693609147e-5
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.690C>T
  hgvsp: ENST00000358373.3:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.332C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.690C>T
  hgvsp: ENST00000341617.3:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.690C>T
  hgvsp: ENST00000457830.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.232C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.690C>T
  hgvsp: ENST00000339582.2:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.120C>T
  hgvsp: ENST00000465844.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.690C>T
  hgvsp: ENST00000444921.2:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.690C>T
  hgvsp: ENST00000405249.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.690C>T
  hgvsp: ENST00000472701.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.444C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser230Ser
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

7-126746587-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746587
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746587
    reference: chr 7
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.444C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.690C>A
  hgvsp: ENSP00000415522.1:p.Ser230Arg
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.690C>A
  hgvsp: ENSP00000345747.3:p.Ser230Arg
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.232C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.120C>A
  hgvsp: ENSP00000418255.1:p.Ser40Arg
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.332C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.690C>A
  hgvsp: ENSP00000419832.1:p.Ser230Arg
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.690C>A
  hgvsp: ENSP00000385731.1:p.Ser230Arg
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.690C>A
  hgvsp: ENSP00000344173.2:p.Ser230Arg
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.690C>A
  hgvsp: ENSP00000351142.3:p.Ser230Arg
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.690C>A
  hgvsp: ENSP00000409790.2:p.Ser230Arg
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser230Arg
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

7-126746591-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746591
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746591
    reference: chr 7
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.686A>T
  hgvsp: ENSP00000351142.3:p.Glu229Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.328A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.686A>T
  hgvsp: ENSP00000344173.2:p.Glu229Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.228A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.686A>T
  hgvsp: ENSP00000415522.1:p.Glu229Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.686A>T
  hgvsp: ENSP00000385731.1:p.Glu229Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.440A>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.116A>T
  hgvsp: ENSP00000418255.1:p.Glu39Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.686A>T
  hgvsp: ENSP00000419832.1:p.Glu229Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.686A>T
  hgvsp: ENSP00000345747.3:p.Glu229Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.686A>T
  hgvsp: ENSP00000409790.2:p.Glu229Val
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12661
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu229Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

7-126746597-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746597
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746597
    reference: chr 7
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.680A>C
  hgvsp: ENSP00000415522.1:p.Tyr227Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.680A>C
  hgvsp: ENSP00000344173.2:p.Tyr227Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.680A>C
  hgvsp: ENSP00000419832.1:p.Tyr227Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.222A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.680A>C
  hgvsp: ENSP00000351142.3:p.Tyr227Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.680A>C
  hgvsp: ENSP00000385731.1:p.Tyr227Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.434A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.680A>C
  hgvsp: ENSP00000345747.3:p.Tyr227Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.680A>C
  hgvsp: ENSP00000409790.2:p.Tyr227Ser
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.322A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.110A>C
  hgvsp: ENSP00000418255.1:p.Tyr37Ser
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr227Ser
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

7-126746606-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746606
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746606
    reference: chr 7
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.671A>C
  hgvsp: ENSP00000415522.1:p.Glu224Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.425A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.671A>C
  hgvsp: ENSP00000344173.2:p.Glu224Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.671A>C
  hgvsp: ENSP00000385731.1:p.Glu224Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.671A>C
  hgvsp: ENSP00000351142.3:p.Glu224Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.313A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.671A>C
  hgvsp: ENSP00000345747.3:p.Glu224Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.671A>C
  hgvsp: ENSP00000419832.1:p.Glu224Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.101A>C
  hgvsp: ENSP00000418255.1:p.Glu34Ala
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.213A>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.671A>C
  hgvsp: ENSP00000409790.2:p.Glu224Ala
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu224Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

7-126746617-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746617
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746617
    reference: chr 7
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.660A>G
  hgvsp: ENST00000339582.2:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.90A>G
  hgvsp: ENST00000465844.1:c.90A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.660A>G
  hgvsp: ENST00000341617.3:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.660A>G
  hgvsp: ENST00000472701.1:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.660A>G
  hgvsp: ENST00000457830.1:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.660A>G
  hgvsp: ENST00000444921.2:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.660A>G
  hgvsp: ENST00000405249.1:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.414A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.660A>G
  hgvsp: ENST00000358373.3:c.660A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.202A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.302A>G
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr220Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS

7-126746621-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746621
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746621
    reference: chr 7
allele count: 2
allele frequency: 1.650519088253256e-5
allele num: 121174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.656C>T
  hgvsp: ENSP00000385731.1:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.656C>T
  hgvsp: ENSP00000419832.1:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.656C>T
  hgvsp: ENSP00000415522.1:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.656C>T
  hgvsp: ENSP00000344173.2:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.656C>T
  hgvsp: ENSP00000409790.2:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.86C>T
  hgvsp: ENSP00000418255.1:p.Ser29Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.656C>T
  hgvsp: ENSP00000351142.3:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.656C>T
  hgvsp: ENSP00000345747.3:p.Ser219Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.298C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.410C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.198C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser219Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-126746626-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746626
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746626
    reference: chr 7
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.405T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.651T>C
  hgvsp: ENST00000457830.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.651T>C
  hgvsp: ENST00000472701.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.651T>C
  hgvsp: ENST00000444921.2:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.651T>C
  hgvsp: ENST00000341617.3:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.651T>C
  hgvsp: ENST00000339582.2:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.651T>C
  hgvsp: ENST00000358373.3:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.651T>C
  hgvsp: ENST00000405249.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.81T>C
  hgvsp: ENST00000465844.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.293T>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.193T>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40277
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr217Tyr
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD

7-126746644-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746644
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746644
    reference: chr 7
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.275A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.175A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.633A>G
  hgvsp: ENST00000405249.1:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.633A>G
  hgvsp: ENST00000472701.1:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.633A>G
  hgvsp: ENST00000457830.1:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.633A>G
  hgvsp: ENST00000341617.3:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.63A>G
  hgvsp: ENST00000465844.1:c.63A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.387A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.633A>G
  hgvsp: ENST00000339582.2:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.633A>G
  hgvsp: ENST00000358373.3:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.633A>G
  hgvsp: ENST00000444921.2:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr211Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

7-126746649-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746649
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746649
    reference: chr 7
allele count: 3
allele frequency: 2.475002475002475e-5
allele num: 121212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.58G>A
  hgvsp: ENSP00000418255.1:p.Val20Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.628G>A
  hgvsp: ENSP00000409790.2:p.Val210Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.628G>A
  hgvsp: ENSP00000344173.2:p.Val210Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.382G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.628G>A
  hgvsp: ENSP00000351142.3:p.Val210Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.628G>A
  hgvsp: ENSP00000415522.1:p.Val210Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.628G>A
  hgvsp: ENSP00000385731.1:p.Val210Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.628G>A
  hgvsp: ENSP00000419832.1:p.Val210Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.628G>A
  hgvsp: ENSP00000345747.3:p.Val210Met
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.270G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.170G>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val210Met
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

7-126746650-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746650
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746650
    reference: chr 7
allele count: 7
allele frequency: 5.774815205913411e-5
allele num: 121216
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.269C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.627C>T
  hgvsp: ENST00000405249.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.627C>T
  hgvsp: ENST00000472701.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.627C>T
  hgvsp: ENST00000341617.3:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.627C>T
  hgvsp: ENST00000358373.3:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.57C>T
  hgvsp: ENST00000465844.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.627C>T
  hgvsp: ENST00000457830.1:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.627C>T
  hgvsp: ENST00000444921.2:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.627C>T
  hgvsp: ENST00000339582.2:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.381C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.169C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ile209Ile
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS

7-126746650-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746650
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746650
    reference: chr 7
allele count: 11
allele frequency: 9.074709609292503e-5
allele num: 121216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.57C>A
  hgvsp: ENST00000465844.1:c.57C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.627C>A
  hgvsp: ENST00000444921.2:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.627C>A
  hgvsp: ENST00000472701.1:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.627C>A
  hgvsp: ENST00000341617.3:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.381C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.627C>A
  hgvsp: ENST00000405249.1:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.627C>A
  hgvsp: ENST00000358373.3:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.627C>A
  hgvsp: ENST00000457830.1:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.169C>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.627C>A
  hgvsp: ENST00000339582.2:c.627C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.269C>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile209Ile
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-126746652-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746652
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746652
    reference: chr 7
allele count: 2
allele frequency: 1.649756660892518e-5
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.625A>G
  hgvsp: ENSP00000351142.3:p.Ile209Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.267A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.625A>G
  hgvsp: ENSP00000344173.2:p.Ile209Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.55A>G
  hgvsp: ENSP00000418255.1:p.Ile19Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.625A>G
  hgvsp: ENSP00000345747.3:p.Ile209Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.625A>G
  hgvsp: ENSP00000419832.1:p.Ile209Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.167A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.625A>G
  hgvsp: ENSP00000409790.2:p.Ile209Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.625A>G
  hgvsp: ENSP00000385731.1:p.Ile209Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.379A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.625A>G
  hgvsp: ENSP00000415522.1:p.Ile209Val
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile209Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

7-126746653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746653
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746653
    reference: chr 7
allele count: 16
allele frequency: 1.31974001121779e-4
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.624C>T
  hgvsp: ENST00000341617.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.624C>T
  hgvsp: ENST00000457830.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.624C>T
  hgvsp: ENST00000358373.3:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.166C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.624C>T
  hgvsp: ENST00000339582.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.624C>T
  hgvsp: ENST00000472701.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.378C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.54C>T
  hgvsp: ENST00000465844.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.624C>T
  hgvsp: ENST00000405249.1:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.266C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.624C>T
  hgvsp: ENST00000444921.2:c.624C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Asp208Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

7-126746654-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746654
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746654
    reference: chr 7
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.623A>G
  hgvsp: ENSP00000419832.1:p.Asp208Gly
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.377A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.265A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.623A>G
  hgvsp: ENSP00000345747.3:p.Asp208Gly
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.623A>G
  hgvsp: ENSP00000344173.2:p.Asp208Gly
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.623A>G
  hgvsp: ENSP00000409790.2:p.Asp208Gly
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.165A>G
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.623A>G
  hgvsp: ENSP00000415522.1:p.Asp208Gly
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.53A>G
  hgvsp: ENSP00000418255.1:p.Asp18Gly
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.623A>G
  hgvsp: ENSP00000351142.3:p.Asp208Gly
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.623A>G
  hgvsp: ENSP00000385731.1:p.Asp208Gly
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp208Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

7-126746658-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746658
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746658
    reference: chr 7
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.619G>C
  hgvsp: ENSP00000415522.1:p.Val207Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.619G>C
  hgvsp: ENSP00000351142.3:p.Val207Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.161G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.619G>C
  hgvsp: ENSP00000345747.3:p.Val207Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.619G>C
  hgvsp: ENSP00000344173.2:p.Val207Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.619G>C
  hgvsp: ENSP00000385731.1:p.Val207Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.619G>C
  hgvsp: ENSP00000419832.1:p.Val207Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.619G>C
  hgvsp: ENSP00000409790.2:p.Val207Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.261G>C
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.49G>C
  hgvsp: ENSP00000418255.1:p.Val17Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.373G>C
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val207Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

7-126746659-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746659
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746659
    reference: chr 7
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.618G>A
  hgvsp: ENSP00000409790.2:p.Met206Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.618G>A
  hgvsp: ENSP00000385731.1:p.Met206Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.48G>A
  hgvsp: ENSP00000418255.1:p.Met16Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.618G>A
  hgvsp: ENSP00000344173.2:p.Met206Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.618G>A
  hgvsp: ENSP00000415522.1:p.Met206Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.618G>A
  hgvsp: ENSP00000345747.3:p.Met206Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.618G>A
  hgvsp: ENSP00000419832.1:p.Met206Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.618G>A
  hgvsp: ENSP00000351142.3:p.Met206Ile
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.260G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.372G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.160G>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met206Ile
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

7-126746663-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746663
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746663
    reference: chr 7
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.614C>T
  hgvsp: ENSP00000345747.3:p.Ala205Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.614C>T
  hgvsp: ENSP00000415522.1:p.Ala205Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.614C>T
  hgvsp: ENSP00000385731.1:p.Ala205Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.256C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.156C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.614C>T
  hgvsp: ENSP00000344173.2:p.Ala205Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.614C>T
  hgvsp: ENSP00000351142.3:p.Ala205Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.614C>T
  hgvsp: ENSP00000419832.1:p.Ala205Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.614C>T
  hgvsp: ENSP00000409790.2:p.Ala205Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.44C>T
  hgvsp: ENSP00000418255.1:p.Ala15Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.368C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala205Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

7-126746669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746669
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746669
    reference: chr 7
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.608C>T
  hgvsp: ENSP00000415522.1:p.Ala203Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.608C>T
  hgvsp: ENSP00000419832.1:p.Ala203Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.608C>T
  hgvsp: ENSP00000409790.2:p.Ala203Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.608C>T
  hgvsp: ENSP00000385731.1:p.Ala203Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.608C>T
  hgvsp: ENSP00000351142.3:p.Ala203Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.362C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.608C>T
  hgvsp: ENSP00000345747.3:p.Ala203Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.608C>T
  hgvsp: ENSP00000344173.2:p.Ala203Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.38C>T
  hgvsp: ENSP00000418255.1:p.Ala13Val
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.250C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.150C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala203Val
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-126746670-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746670
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746670
    reference: chr 7
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.607G>A
  hgvsp: ENSP00000345747.3:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.607G>A
  hgvsp: ENSP00000409790.2:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.607G>A
  hgvsp: ENSP00000385731.1:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.361G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.249G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.607G>A
  hgvsp: ENSP00000415522.1:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.37G>A
  hgvsp: ENSP00000418255.1:p.Ala13Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.607G>A
  hgvsp: ENSP00000419832.1:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.607G>A
  hgvsp: ENSP00000351142.3:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.607G>A
  hgvsp: ENSP00000344173.2:p.Ala203Thr
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.149G>A
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala203Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/7-126746686-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746686
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746686
    reference: chr 7
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.591G>T
  hgvsp: ENST00000339582.2:c.591G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.591G>T
  hgvsp: ENST00000358373.3:c.591G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.345G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.21G>T
  hgvsp: ENST00000465844.1:c.21G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.133G>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.591G>T
  hgvsp: ENST00000405249.1:c.591G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.591G>T
  hgvsp: ENST00000341617.3:c.591G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.591G>T
  hgvsp: ENST00000472701.1:c.591G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.591G>T
  hgvsp: ENST00000444921.2:c.591G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.591G>T
  hgvsp: ENST00000457830.1:c.591G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.233G>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro197Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

7-126746686-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746686
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746686
    reference: chr 7
allele count: 2
allele frequency: 1.649402916144356e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.21G>A
  hgvsp: ENST00000465844.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.591G>A
  hgvsp: ENST00000341617.3:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.345G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.591G>A
  hgvsp: ENST00000457830.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.133G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.233G>A
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.591G>A
  hgvsp: ENST00000405249.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.591G>A
  hgvsp: ENST00000444921.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.591G>A
  hgvsp: ENST00000472701.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.591G>A
  hgvsp: ENST00000339582.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.591G>A
  hgvsp: ENST00000358373.3:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro197Pro
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

7-126746687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746687
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 126746687
    reference: chr 7
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000344173
  ensembl transcript: ENST00000339582
  gene symbol: GRM8
  hgvsc: ENST00000339582.2:c.590C>T
  hgvsp: ENSP00000344173.2:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000419832
  ensembl transcript: ENST00000472701
  gene symbol: GRM8
  hgvsc: ENST00000472701.1:c.590C>T
  hgvsp: ENSP00000419832.1:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000473254
  gene symbol: GRM8
  hgvsc: ENST00000473254.1:n.344C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000351142
  ensembl transcript: ENST00000358373
  gene symbol: GRM8
  hgvsc: ENST00000358373.3:c.590C>T
  hgvsp: ENSP00000351142.3:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000345747
  ensembl transcript: ENST00000341617
  gene symbol: GRM8
  hgvsc: ENST00000341617.3:c.590C>T
  hgvsp: ENSP00000345747.3:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000415522
  ensembl transcript: ENST00000457830
  gene symbol: GRM8
  hgvsc: ENST00000457830.1:c.590C>T
  hgvsp: ENSP00000415522.1:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000385731
  ensembl transcript: ENST00000405249
  gene symbol: GRM8
  hgvsc: ENST00000405249.1:c.590C>T
  hgvsp: ENSP00000385731.1:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000409790
  ensembl transcript: ENST00000444921
  gene symbol: GRM8
  hgvsc: ENST00000444921.2:c.590C>T
  hgvsp: ENSP00000409790.2:p.Pro197Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000179603
  ensembl protein: ENSP00000418255
  ensembl transcript: ENST00000465844
  gene symbol: GRM8
  hgvsc: ENST00000465844.1:c.20C>T
  hgvsp: ENSP00000418255.1:p.Pro7Leu
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000448250
  gene symbol: GRM8
  hgvsc: ENST00000448250.2:n.132C>T
  variant of: http://identifiers.org/hgnc/4600
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000179603
  ensembl transcript: ENST00000480995
  gene symbol: GRM8
  hgvsc: ENST00000480995.1:n.232C>T
  variant of: http://identifiers.org/hgnc/4600
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro197Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/7-126746692-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 126746692
    reference: chr 7
allele count: 13
allele frequency: 1.072129579230376e-4
allele num: 121254
alternate allele: A
canonical: true
consequence: synonymous
filter: PASS
hgvs: p.Val195Val
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 243
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2263
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25512
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6956
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11986
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.742160278745645e-3
allele num: 574
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.082229e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

QD
type: SiteQuality
SIO_000300: 1.466e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

GenotypeQuality
all individuals: 2072
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26293
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 800
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38950
num of homozygotes: 0

Latino
type: Population
allele count: 25
allele frequency: 3.470294280955025e-3
allele num: 7204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12062
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

QD
type: SiteQuality
SIO_000300: 1.085e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
type: SiteQuality
SIO_000300: 6.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

DP
type: SiteQuality
SIO_000300: 1.093956e6

BaseQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

GenotypeQuality
all individuals: 579
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26478
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 533
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.256281407035176e-4
allele num: 7960
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 39998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

MQRankSum
type: SiteQuality
SIO_000300: -4.51e-1

FS
type: SiteQuality
SIO_000300: 3.262e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.851e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

QD
type: SiteQuality
SIO_000300: 1.122e1

DP
type: SiteQuality
SIO_000300: 1.111793e6

GenotypeQuality
all individuals: 493
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 785
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18952
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26478
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 962
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7960
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.500125006250312e-5
allele num: 39998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.111793e6

FS
type: SiteQuality
SIO_000300: 3.262e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

QD
type: SiteQuality
SIO_000300: 1.122e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.851e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 9.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
all individuals: 2401
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2214
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 755
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18752
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40600
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.745318352059925e-4
allele num: 8010
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6852
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: 4.45e-1

FS
type: SiteQuality
SIO_000300: 3.518e0

QD
type: SiteQuality
SIO_000300: 9.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.31e-1

DP
type: SiteQuality
SIO_000300: 1.119085e6

GenotypeQuality
all individuals: 29782
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1604
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17133
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 450
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2214
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4252
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.62877244954638e-5
allele num: 43208
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.216e0

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 1.161253e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 1.219e0

VQSLOD
type: SiteQuality
SIO_000300: -6.370000000000001e-2

QD
type: SiteQuality
SIO_000300: 2.069e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 802
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 30269
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2217
bin: 9.75e1
variant carriers: 7

Latino
type: Population
allele count: 5
allele frequency: 5.9509640561771e-4
allele num: 8402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.879787185249737e-5
allele num: 43606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4292
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12708
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

DP
type: SiteQuality
SIO_000300: 1.168219e6

FS
type: SiteQuality
SIO_000300: 5.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
SIO_000300: 8.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

GenotypeQuality
all individuals: 517
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2211
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30667
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2562
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12748
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.277696793002915e-5
allele num: 43904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

DP
type: SiteQuality
SIO_000300: 1.170016e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.959e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e0

QD
type: SiteQuality
SIO_000300: 8.470000000000001e0

GenotypeQuality
all individuals: 177
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17563
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7238
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.874015748031496e-5
allele num: 12700
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.122e0

QD
type: SiteQuality
SIO_000300: 1.074e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.39e-1

DP
type: SiteQuality
SIO_000300: 1.161365e6

VQSLOD
type: SiteQuality
SIO_000300: -2.351e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.317e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.37e-1

GenotypeQuality
all individuals: 921
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18520
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1851
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 780
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 964
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.310215774153306e-5
allele num: 43286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4198
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.05e0

DP
type: SiteQuality
SIO_000300: 1.14499e6

FS
type: SiteQuality
SIO_000300: 8.129e0

QD
type: SiteQuality
SIO_000300: 1.285e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

MQ
type: SiteQuality
SIO_000300: 5.734e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.592e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.98e-1

GenotypeQuality
all individuals: 943
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 749
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25680
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12590
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.233045622688039e-4
allele num: 8110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42490
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.508e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

QD
type: SiteQuality
SIO_000300: 1.229e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

FS
type: SiteQuality
SIO_000300: 1.935e0

DP
type: SiteQuality
SIO_000300: 1.12036e6

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

GenotypeQuality
all individuals: 924
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 936
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2209
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8070
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4076
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.422070534698521e-4
allele num: 7032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42502
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.138e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 1.121086e6

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeQuality
all individuals: 1449
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8273
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 849
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7842
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2846
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.846381093057607e-4
allele num: 5416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2906
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.429999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.011e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.49e-2

DP
type: SiteQuality
SIO_000300: 8.44565e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeQuality
all individuals: 215
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25622
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6896
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9402
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5122
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.460280373831776e-4
allele num: 6848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5168
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2746
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e-1

QD
type: SiteQuality
SIO_000300: 8.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.22628e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

FS
type: SiteQuality
SIO_000300: 1.0866e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.617e0

VQSLOD
type: SiteQuality
SIO_000300: -1.32e0

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

GenotypeQuality
all individuals: 2702
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9964
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2182
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24519
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5000
num of homozygotes: 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: 2588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4916
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.479289940828402e-4
allele num: 6760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30612
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

DP
type: SiteQuality
SIO_000300: 8.10953e5

QD
type: SiteQuality
SIO_000300: 9.140000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -6.283e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.498e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.23e-1

FS
type: SiteQuality
SIO_000300: 1.932e0

GenotypeQuality
all individuals: 727
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2817
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10701
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2205
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6094
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2656
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.364511136531862e-5
allele num: 29722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.22e0

QD
type: SiteQuality
SIO_000300: 2.398e1

DP
type: SiteQuality
SIO_000300: 7.9939e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.95e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.132e0

GenotypeQuality
all individuals: 400
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 835
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 918
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2578
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5403
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3617
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2735
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2583
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27370
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.54841997961264e-4
allele num: 3924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4412
num of homozygotes: 0

African
type: Population
allele count: 32
allele frequency: 5.06168933881683e-3
allele num: 6322
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.27e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.44e-1

DP
type: SiteQuality
SIO_000300: 7.67983e5

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.338e1

GenotypeQuality
all individuals: 18562
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4431
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13445
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2202
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.817085273685014e-5
allele num: 26198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2206
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.443e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.52e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

MQRankSum
type: SiteQuality
SIO_000300: -2.367e0

DP
type: SiteQuality
SIO_000300: 7.56535e5

QD
type: SiteQuality
SIO_000300: 1.035e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 961
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 300
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.189072609633358e-4
allele num: 2782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.04e-2

FS
type: SiteQuality
SIO_000300: 8.125999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.314e-1

DP
type: SiteQuality
SIO_000300: 1.17515e5

GenotypeQuality
all individuals: 535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1692
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3915
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.394433129667345e-4
allele num: 2946
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.922e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

DP
type: SiteQuality
SIO_000300: 1.34772e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.33e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.04e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.87e-1

QD
type: SiteQuality
SIO_000300: 1.516e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4126
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 581
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7426
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.175e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 1.38026e5

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 577
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.330849081714134e-4
allele num: 7514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.9026e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.67e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.701e0

DP
type: SiteQuality
SIO_000300: 1.40726e5

MQRankSum
type: SiteQuality
SIO_000300: 6.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

QD
type: SiteQuality
SIO_000300: 7.66e0

GenotypeQuality
all individuals: 1753
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 518
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 603
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 8.720930232558139e-3
allele num: 344
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.62e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.03e0

DP
type: SiteQuality
SIO_000300: 1.42319e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.594e0

FS
type: SiteQuality
SIO_000300: 1.115e0

QD
type: SiteQuality
SIO_000300: 1.142e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.067e0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 550
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.75e1
variant carriers: 7

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.976670201484624e-4
allele num: 7544
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 1.694915254237288e-2
allele num: 118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.406149903907751e-4
allele num: 3122
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.403e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.41096e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.56e-1

FS
type: SiteQuality
SIO_000300: 6.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.49e0

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

GenotypeQuality
all individuals: 113
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 152
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 498
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 4

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.675567423230974e-4
allele num: 2996
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 6.666666666666667e-3
allele num: 150
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.703433360367667e-4
allele num: 7398
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.668e0

QD
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.127e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.07e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.40624e5

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 582
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.359434475258292e-4
allele num: 7356
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.40912e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.06e-2

FS
type: SiteQuality
SIO_000300: 3.023e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

VQSLOD
type: SiteQuality
SIO_000300: -2.722e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.098e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 143
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 564
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2976
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

FS
type: SiteQuality
SIO_000300: 8.845000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.27e-2

QD
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.64e-1

DP
type: SiteQuality
SIO_000300: 1.41529e5

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 11

GenotypeQuality
all individuals: 46
bin: 8.75e1
variant carriers: 45

GenotypeQuality
all individuals: 209
bin: 6.75e1
variant carriers: 44

GenotypeQuality
all individuals: 409
bin: 2.25e1
variant carriers: 45

GenotypeQuality
all individuals: 114
bin: 2.75e1
variant carriers: 45

GenotypeQuality
all individuals: 82
bin: 7.75e1
variant carriers: 58

GenotypeQuality
all individuals: 963
bin: 7.5e0
variant carriers: 109

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 65

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 57

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 27

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 27

GenotypeQuality
all individuals: 2714
bin: 9.75e1
variant carriers: 2713

GenotypeQuality
all individuals: 62
bin: 8.25e1
variant carriers: 51

GenotypeQuality
all individuals: 1918
bin: 6.25e1
variant carriers: 35

GenotypeQuality
all individuals: 51
bin: 7.25e1
variant carriers: 29

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 23

GenotypeQuality
all individuals: 94
bin: 9.25e1
variant carriers: 93

South Asian
type: Population
allele count: 2150
allele frequency: 2.886680988184748e-1
allele num: 7448
num of homozygotes: 336

Latino
type: Population
allele count: 45
allele frequency: 3.879310344827586e-1
allele num: 116
num of homozygotes: 7

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

East Asian
type: Population
allele count: 25
allele frequency: 1.644736842105263e-1
allele num: 152
num of homozygotes: 1

Other
type: Population
allele count: 52
allele frequency: 4.333333333333333e-1
allele num: 120
num of homozygotes: 12

European (Non-Finnish)
type: Population
allele count: 1282
allele frequency: 4.22266139657444e-1
allele num: 3036
num of homozygotes: 279

African
type: Population
allele count: 187
allele frequency: 5.565476190476191e-1
allele num: 336
num of homozygotes: 42

DP
type: SiteQuality
SIO_000300: 1.64616e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.366e0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.75e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.36e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.801e1

GenotypeQuality
all individuals: 1677
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1018
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3304
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 109
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.433962264150943e-3
allele num: 106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7338
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 1.32993e5

QD
type: SiteQuality
SIO_000300: 1.593e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.214e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
all individuals: 1689
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.385425325574952e-4
allele num: 7218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 112
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2736
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.83e0

DP
type: SiteQuality
SIO_000300: 1.16815e5

QD
type: SiteQuality
SIO_000300: 1.187e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.79e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

GenotypeQuality
all individuals: 1092
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5039
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 313
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9535
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6836
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1522
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2852
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3467
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3792
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7450
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3179
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6640
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 988
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7672
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9500
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5724
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.650709805216243e-5
allele num: 60580
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.871e1

VQSLOD
type: SiteQuality
SIO_000300: -2.764e0

MQRankSum
type: SiteQuality
SIO_000300: 4.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.125e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.084e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
type: SiteQuality
SIO_000300: 1.162553e6

GenotypeQuality
all individuals: 785
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3472
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6808
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5375
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3180
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 282
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2841
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7358
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3782
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.712600027126e-4
allele num: 14746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.171043e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e0

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

GenotypeQuality
all individuals: 533
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5608
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3578
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7260
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5302
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2352
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3176
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15733
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60752
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.187167e6

VQSLOD
type: SiteQuality
SIO_000300: -2.201e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.666e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

QD
type: SiteQuality
SIO_000300: 2.028e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 424
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6700
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16960
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4692
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7078
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5614
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3178
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.740341106856944e-4
allele num: 5746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7712
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.443e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.197334e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.416e0

GenotypeQuality
all individuals: 3076
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6390
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 832
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2627
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3183
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 205
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21527
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5604
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3194
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3169
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6339
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14880
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7724
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.568791670772161e-5
allele num: 60894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.357e1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.229791e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.062e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

GenotypeQuality
all individuals: 950
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6077
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3181
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5553
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2813
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2429
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6266
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22008
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.636232737744617e-5
allele num: 61116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14936
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7772
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.021e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.276e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

DP
type: SiteQuality
SIO_000300: 1.237466e6

GenotypeQuality
all individuals: 5540
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4840
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26880
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2894
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1748
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3415
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3184
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14988
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.264133698916308e-5
allele num: 61272
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7790
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.067e0

FS
type: SiteQuality
SIO_000300: 6.338e0

DP
type: SiteQuality
SIO_000300: 1.275376e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

GenotypeDepth
all individuals: 168
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47172
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.026542780182198e-5
allele num: 66082
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

QD
type: SiteQuality
SIO_000300: 1.195e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 3.754e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.96e-1

DP
type: SiteQuality
SIO_000300: 1.515061e6

GenotypeDepth
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4963
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3193
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 47703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507840772014475e-5
allele num: 66320
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.643e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.115e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.55e-1

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.523271e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

GenotypeDepth
all individuals: 140
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4989
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47829
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 406
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3196
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -7.86e-1

DP
type: SiteQuality
SIO_000300: 1.525383e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

FS
type: SiteQuality
SIO_000300: 7.4e-1

QD
type: SiteQuality
SIO_000300: 1.516e1

GenotypeDepth
all individuals: 207
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 4989
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 107
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47829
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3196
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66372
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.516e1

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 7.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.525383e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

GenotypeDepth
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 283
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1152
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5054
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3200
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 311
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.511956685215822e-5
allele num: 66490
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.530132e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.049e0

VQSLOD
type: SiteQuality
SIO_000300: 8.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.357e0

QD
type: SiteQuality
SIO_000300: 1.243e1

GenotypeDepth
all individuals: 103
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 285
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3197
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5066
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.47e-1

FS
type: SiteQuality
SIO_000300: 3.898e0

MQRankSum
type: SiteQuality
SIO_000300: -3.35e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

DP
type: SiteQuality
SIO_000300: 1.530216e6

QD
type: SiteQuality
SIO_000300: 1.422e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

GenotypeDepth
all individuals: 423
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 407
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5111
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3195
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 312
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66576
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.546e0

MQRankSum
type: SiteQuality
SIO_000300: -1.056e0

DP
type: SiteQuality
SIO_000300: 1.53422e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.327e0

QD
type: SiteQuality
SIO_000300: 1.316e1

GenotypeDepth
all individuals: 81
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 5063
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 9.75e1
variant carriers: 474

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47876
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 612
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.051429944724826e-4
allele num: 66576
num of homozygotes: 0

African
type: Population
allele count: 460
allele frequency: 4.423927678399692e-2
allele num: 10398
num of homozygotes: 14

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.212389380530973e-3
allele num: 904
num of homozygotes: 0

Latino
type: Population
allele count: 21
allele frequency: 1.833100558659218e-3
allele num: 11456
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.56e0

QD
type: SiteQuality
SIO_000300: 1.219e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.06e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.554554e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.33e-2

GenotypeDepth
all individuals: 607
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5121
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3208
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48141
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213886865744113e-4
allele num: 16476
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.540178e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeDepth
all individuals: 82
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3208
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5121
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48141
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 311
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.721437292865864e-5
allele num: 11466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

MQRankSum
type: SiteQuality
SIO_000300: -1.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 1.507e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.23e-1

DP
type: SiteQuality
SIO_000300: 1.540178e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeDepth
all individuals: 205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.95e-1

QD
type: SiteQuality
SIO_000300: 6.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.399e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.684e0

VQSLOD
type: SiteQuality
SIO_000300: -9.019e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

DP
type: SiteQuality
SIO_000300: 1.540196e6

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48268
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1214
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5143
bin: 6.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.968e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.61e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.508e1

DP
type: SiteQuality
SIO_000300: 1.541095e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.445e0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

GenotypeDepth
all individuals: 3332
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48237
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5155
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

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

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

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.046e0

QD
type: SiteQuality
SIO_000300: 9.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.93e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 2.819e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

DP
type: SiteQuality
SIO_000300: 1.542051e6

GenotypeDepth
all individuals: 82
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5155
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 48239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.542751e6

VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

QD
type: SiteQuality
SIO_000300: 1.079e1

MQRankSum
type: SiteQuality
SIO_000300: 8.27e-1

FS
type: SiteQuality
SIO_000300: 1.956e0

GenotypeDepth
all individuals: 210
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 627
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48257
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5161
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.36e-2

FS
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.54346e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.497e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

GenotypeDepth
all individuals: 594
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 116
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48301
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 625
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66634
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.710801393728223e-5
allele num: 11480
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.543457e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.921e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.21e0

MQ
type: SiteQuality
SIO_000300: 5.837e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.199e1

GenotypeDepth
all individuals: 121
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1201
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5169
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48292
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.84e-1

MQ
type: SiteQuality
SIO_000300: 5.837e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.901e0

QD
type: SiteQuality
SIO_000300: 1.044e1

FS
type: SiteQuality
SIO_000300: 3.855e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.456e0

DP
type: SiteQuality
SIO_000300: 1.544418e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
all individuals: 283
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1200
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 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: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.741553465691397e-4
allele num: 11484
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.54e-1

DP
type: SiteQuality
SIO_000300: 1.544951e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.91e0

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

QD
type: SiteQuality
SIO_000300: 9.49e0

GenotypeDepth
all individuals: 598
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48329
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5177
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 6
allele frequency: 6.938020351526364e-4
allele num: 8648
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

DP
type: SiteQuality
SIO_000300: 1.545762e6

QD
type: SiteQuality
SIO_000300: 1.27e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

FS
type: SiteQuality
SIO_000300: 2.493e0

GenotypeDepth
all individuals: 122
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3223
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48329
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5177
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 10
allele frequency: 6.058403004967891e-4
allele num: 16506
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.545762e6

FS
type: SiteQuality
SIO_000300: 2.493e0

QD
type: SiteQuality
SIO_000300: 1.27e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.81e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-1

GenotypeDepth
all individuals: 282
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48347
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3208
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5176
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

African
type: Population
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: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.545085e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-2

QD
type: SiteQuality
SIO_000300: 1.245e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.46e-1

GenotypeDepth
all individuals: 3376
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48334
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3220
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1196
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.040462427745665e-3
allele num: 8650
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 7
allele frequency: 4.240368306275745e-4
allele num: 16508
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.991e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.752e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

DP
type: SiteQuality
SIO_000300: 1.546391e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.197e1

GenotypeDepth
all individuals: 282
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 307
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 1

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: 8650
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.815e0

FS
type: SiteQuality
SIO_000300: 6.868e0

VQSLOD
type: SiteQuality
SIO_000300: -1.306e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
SIO_000300: 1.306e1

DP
type: SiteQuality
SIO_000300: 1.545263e6

GenotypeDepth
all individuals: 105
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 627
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 77
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1196
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48362
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5183
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 7.25e1
variant carriers: 0

African
type: Population
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: 16502
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 3.315e0

DP
type: SiteQuality
SIO_000300: 1.54563e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.01e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-3

QD
type: SiteQuality
SIO_000300: 1.665e1

VQSLOD
type: SiteQuality
SIO_000300: -2.988e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5182
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 628
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1195
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3205
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1171
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48362
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 11482
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

DP
type: SiteQuality
SIO_000300: 1.545664e6

QD
type: SiteQuality
SIO_000300: 1.09e1

FS
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.181e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.062e0

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-1

GenotypeDepth
all individuals: 81
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48374
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3206
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5169
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.545644e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e-1

FS
type: SiteQuality
SIO_000300: 8.702999999999999e0

QD
type: SiteQuality
SIO_000300: 1.051e1

VQSLOD
type: SiteQuality
SIO_000300: -3.973e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

GenotypeDepth
all individuals: 205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5171
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48384
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3208
bin: 9.75e1
variant carriers: 1

African
type: Population
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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 7.856e0

MQ
type: SiteQuality
SIO_000300: 5.88e1

VQSLOD
type: SiteQuality
SIO_000300: -2.695e0

DP
type: SiteQuality
SIO_000300: 1.54583e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.406e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.086e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.028e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeDepth
all individuals: 70
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5168
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
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: 66668
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.545954e6

MQRankSum
type: SiteQuality
SIO_000300: -9.320000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.937e0

FS
type: SiteQuality
SIO_000300: 4.114e0

VQSLOD
type: SiteQuality
SIO_000300: 3.98e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.58e-1

QD
type: SiteQuality
SIO_000300: 1.222e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

GenotypeDepth
all individuals: 120
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48357
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

African
type: Population
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: 66684
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-1

QD
type: SiteQuality
SIO_000300: 1.18e1

FS
type: SiteQuality
SIO_000300: 7.912e0

VQSLOD
type: SiteQuality
SIO_000300: -8.35e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

DP
type: SiteQuality
SIO_000300: 1.546367e6

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1190
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 2
allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.18e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

FS
type: SiteQuality
SIO_000300: 7.912e0

VQSLOD
type: SiteQuality
SIO_000300: -8.35e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.546367e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeDepth
all individuals: 281
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3207
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 84
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e-1

QD
type: SiteQuality
SIO_000300: 6.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.524e0

DP
type: SiteQuality
SIO_000300: 1.546237e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e-1