6-34007961-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34007961
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34007961
    reference: chr 6
allele count: 2
allele frequency: 1.649675014022238e-5
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1101C>A
  hgvsp: ENSP00000477466.1:p.His367Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1152C>A
  hgvsp: ENSP00000363292.3:p.His384Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1975C>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1080C>A
  hgvsp: ENSP00000398456.2:p.His360Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1101C>A
  hgvsp: ENSP00000437925.1:p.His367Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.993C>A
  hgvsp: ENSP00000437730.1:p.His331Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1500C>A
  hgvsp: ENSP00000363296.3:p.His500Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1054C>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1500C>A
  hgvsp: ENSP00000440556.1:p.His500Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*737C>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17646
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His500Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

6-34007967-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34007967
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34007967
    reference: chr 6
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1095C>G
  hgvsp: ENSP00000477466.1:p.His365Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1494C>G
  hgvsp: ENSP00000363296.3:p.His498Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1074C>G
  hgvsp: ENSP00000398456.2:p.His358Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1146C>G
  hgvsp: ENSP00000363292.3:p.His382Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1095C>G
  hgvsp: ENSP00000437925.1:p.His365Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.987C>G
  hgvsp: ENSP00000437730.1:p.His329Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*731C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1494C>G
  hgvsp: ENSP00000440556.1:p.His498Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1048C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1969C>G
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17646
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His498Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

6-34007979-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34007979
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34007979
    reference: chr 6
allele count: 3
allele frequency: 2.471984179301253e-5
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1482C>T
  hgvsp: ENST00000538487.2:c.1482C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1083C>T
  hgvsp: ENST00000535756.1:c.1083C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*719C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1062C>T
  hgvsp: ENST00000455714.2:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1957C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.975C>T
  hgvsp: ENST00000544773.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1482C>T
  hgvsp: ENST00000374181.4:c.1482C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1083C>T
  hgvsp: ENST00000609222.1:c.1083C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1036C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1134C>T
  hgvsp: ENST00000374177.3:c.1134C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17647
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser494Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

6-34007993-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34007993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34007993
    reference: chr 6
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1022A>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.961A>C
  hgvsp: ENSP00000437730.1:p.Lys321Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1069A>C
  hgvsp: ENSP00000437925.1:p.Lys357Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1468A>C
  hgvsp: ENSP00000440556.1:p.Lys490Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1048A>C
  hgvsp: ENSP00000398456.2:p.Lys350Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1069A>C
  hgvsp: ENSP00000477466.1:p.Lys357Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1120A>C
  hgvsp: ENSP00000363292.3:p.Lys374Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1943A>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*705A>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1468A>C
  hgvsp: ENSP00000363296.3:p.Lys490Gln
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17648
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys490Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

6-34007997-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34007997
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34007997
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1044G>C
  hgvsp: ENSP00000398456.2:p.Glu348Asp
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1065G>C
  hgvsp: ENSP00000477466.1:p.Glu355Asp
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*701G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1464G>C
  hgvsp: ENSP00000363296.3:p.Glu488Asp
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1065G>C
  hgvsp: ENSP00000437925.1:p.Glu355Asp
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1464G>C
  hgvsp: ENSP00000440556.1:p.Glu488Asp
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1939G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.957G>C
  hgvsp: ENSP00000437730.1:p.Glu319Asp
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1018G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1116G>C
  hgvsp: ENSP00000363292.3:p.Glu372Asp
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17649
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu488Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-34008000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008000
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008000
    reference: chr 6
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1461C>T
  hgvsp: ENST00000374181.4:c.1461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1062C>T
  hgvsp: ENST00000609222.1:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1936C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1113C>T
  hgvsp: ENST00000374177.3:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1062C>T
  hgvsp: ENST00000535756.1:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1041C>T
  hgvsp: ENST00000455714.2:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*698C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1015C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.954C>T
  hgvsp: ENST00000544773.2:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1461C>T
  hgvsp: ENST00000538487.2:c.1461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2941
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17649
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala487Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

6-34008006-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008006
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008006
    reference: chr 6
allele count: 38960
allele frequency: 3.210548001648125e-1
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1107T>C
  hgvsp: ENST00000374177.3:c.1107T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1035T>C
  hgvsp: ENST00000455714.2:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1455T>C
  hgvsp: ENST00000538487.2:c.1455T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.948T>C
  hgvsp: ENST00000544773.2:c.948T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1455T>C
  hgvsp: ENST00000374181.4:c.1455T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1930T>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1056T>C
  hgvsp: ENST00000609222.1:c.1056T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1009T>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*692T>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1056T>C
  hgvsp: ENST00000535756.1:c.1056T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 5.25e1
  variant carriers: 192
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 6.75e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 8.75e1
  variant carriers: 493
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 4.75e1
  variant carriers: 163
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 4.25e1
  variant carriers: 133
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 8.25e1
  variant carriers: 465
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.75e1
  variant carriers: 246
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 2.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 7.75e1
  variant carriers: 364
genotype depth: GenotypeDepth
  all individuals: 29007
  bin: 9.75e1
  variant carriers: 26976
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.25e1
  variant carriers: 383
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 6.25e1
  variant carriers: 287
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 9.25e1
  variant carriers: 595
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Asp485Asp
num of homozygotes: 8037
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum

6-34008008-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008008
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008008
    reference: chr 6
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1007G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1453G>A
  hgvsp: ENSP00000363296.3:p.Asp485Asn
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1054G>A
  hgvsp: ENSP00000477466.1:p.Asp352Asn
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1928G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1054G>A
  hgvsp: ENSP00000437925.1:p.Asp352Asn
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1033G>A
  hgvsp: ENSP00000398456.2:p.Asp345Asn
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.946G>A
  hgvsp: ENSP00000437730.1:p.Asp316Asn
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*690G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1453G>A
  hgvsp: ENSP00000440556.1:p.Asp485Asn
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1105G>A
  hgvsp: ENSP00000363292.3:p.Asp369Asn
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4454
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp485Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

6-34008013-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008013
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008013
    reference: chr 6
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1049G>A
  hgvsp: ENSP00000437925.1:p.Arg350His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1002G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.941G>A
  hgvsp: ENSP00000437730.1:p.Arg314His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1448G>A
  hgvsp: ENSP00000363296.3:p.Arg483His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1028G>A
  hgvsp: ENSP00000398456.2:p.Arg343His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1448G>A
  hgvsp: ENSP00000440556.1:p.Arg483His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1049G>A
  hgvsp: ENSP00000477466.1:p.Arg350His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*685G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1923G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1100G>A
  hgvsp: ENSP00000363292.3:p.Arg367His
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6198
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg483His
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP

6-34008014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008014
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008014
    reference: chr 6
allele count: 267
allele frequency: 2.199232327891537e-3
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1922C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1447C>T
  hgvsp: ENSP00000440556.1:p.Arg483Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*684C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1048C>T
  hgvsp: ENSP00000477466.1:p.Arg350Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1447C>T
  hgvsp: ENSP00000363296.3:p.Arg483Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1027C>T
  hgvsp: ENSP00000398456.2:p.Arg343Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.940C>T
  hgvsp: ENSP00000437730.1:p.Arg314Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1099C>T
  hgvsp: ENSP00000363292.3:p.Arg367Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1048C>T
  hgvsp: ENSP00000437925.1:p.Arg350Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1001C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5941
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 9.75e1
  variant carriers: 249
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg483Cys
num of homozygotes: 5
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

6-34008015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008015
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008015
    reference: chr 6
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1446G>A
  hgvsp: ENST00000374181.4:c.1446G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1047G>A
  hgvsp: ENST00000609222.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1026G>A
  hgvsp: ENST00000455714.2:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.1000G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1446G>A
  hgvsp: ENST00000538487.2:c.1446G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1098G>A
  hgvsp: ENST00000374177.3:c.1098G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.939G>A
  hgvsp: ENST00000544773.2:c.939G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*683G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1921G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1047G>A
  hgvsp: ENST00000535756.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4099
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu482Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-34008018-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008018
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008018
    reference: chr 6
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1044G>C
  hgvsp: ENSP00000437925.1:p.Gln348His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.936G>C
  hgvsp: ENSP00000437730.1:p.Gln312His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1443G>C
  hgvsp: ENSP00000363296.3:p.Gln481His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*680G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.997G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1443G>C
  hgvsp: ENSP00000440556.1:p.Gln481His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1023G>C
  hgvsp: ENSP00000398456.2:p.Gln341His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1918G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1044G>C
  hgvsp: ENSP00000477466.1:p.Gln348His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1095G>C
  hgvsp: ENSP00000363292.3:p.Gln365His
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1953
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1813
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln481His
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

6-34008024-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008024
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008024
    reference: chr 6
allele count: 2
allele frequency: 1.647337901950448e-5
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*674A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1437A>G
  hgvsp: ENST00000374181.4:c.1437A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1017A>G
  hgvsp: ENST00000455714.2:c.1017A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.930A>G
  hgvsp: ENST00000544773.2:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1437A>G
  hgvsp: ENST00000538487.2:c.1437A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1089A>G
  hgvsp: ENST00000374177.3:c.1089A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1038A>G
  hgvsp: ENST00000535756.1:c.1038A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.991A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1038A>G
  hgvsp: ENST00000609222.1:c.1038A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1912A>G
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45991
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gln479Gln
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: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

6-34008032-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008032
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008032
    reference: chr 6
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1429A>G
  hgvsp: ENSP00000440556.1:p.Ile477Val
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1904A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*666A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1081A>G
  hgvsp: ENSP00000363292.3:p.Ile361Val
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.922A>G
  hgvsp: ENSP00000437730.1:p.Ile308Val
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1030A>G
  hgvsp: ENSP00000477466.1:p.Ile344Val
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1429A>G
  hgvsp: ENSP00000363296.3:p.Ile477Val
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1030A>G
  hgvsp: ENSP00000437925.1:p.Ile344Val
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1009A>G
  hgvsp: ENSP00000398456.2:p.Ile337Val
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.983A>G
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45991
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile477Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

6-34008039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008039
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008039
    reference: chr 6
allele count: 4
allele frequency: 3.294730079238259e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.976C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1074C>T
  hgvsp: ENST00000374177.3:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1023C>T
  hgvsp: ENST00000535756.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1897C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.915C>T
  hgvsp: ENST00000544773.2:c.915C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1023C>T
  hgvsp: ENST00000609222.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1002C>T
  hgvsp: ENST00000455714.2:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1422C>T
  hgvsp: ENST00000538487.2:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1422C>T
  hgvsp: ENST00000374181.4:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*659C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg474Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

6-34008040-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008040
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008040
    reference: chr 6
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1001G>A
  hgvsp: ENSP00000398456.2:p.Arg334His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1421G>A
  hgvsp: ENSP00000363296.3:p.Arg474His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1073G>A
  hgvsp: ENSP00000363292.3:p.Arg358His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1022G>A
  hgvsp: ENSP00000477466.1:p.Arg341His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1421G>A
  hgvsp: ENSP00000440556.1:p.Arg474His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1022G>A
  hgvsp: ENSP00000437925.1:p.Arg341His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*658G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.914G>A
  hgvsp: ENSP00000437730.1:p.Arg305His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1896G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.975G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg474His
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-34008041-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008041
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008041
    reference: chr 6
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1420C>T
  hgvsp: ENSP00000363296.3:p.Arg474Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.913C>T
  hgvsp: ENSP00000437730.1:p.Arg305Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1072C>T
  hgvsp: ENSP00000363292.3:p.Arg358Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1420C>T
  hgvsp: ENSP00000440556.1:p.Arg474Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.1000C>T
  hgvsp: ENSP00000398456.2:p.Arg334Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1021C>T
  hgvsp: ENSP00000477466.1:p.Arg341Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*657C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1895C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1021C>T
  hgvsp: ENSP00000437925.1:p.Arg341Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.974C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg474Cys
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

6-34008048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008048
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008048
    reference: chr 6
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.1014G>A
  hgvsp: ENST00000535756.1:c.1014G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.993G>A
  hgvsp: ENST00000455714.2:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.1014G>A
  hgvsp: ENST00000609222.1:c.1014G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.906G>A
  hgvsp: ENST00000544773.2:c.906G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.967G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1413G>A
  hgvsp: ENST00000374181.4:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*650G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1065G>A
  hgvsp: ENST00000374177.3:c.1065G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1413G>A
  hgvsp: ENST00000538487.2:c.1413G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1888G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala471Ala
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-34008064-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008064
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008064
    reference: chr 6
allele count: 3
allele frequency: 2.472024918011174e-5
allele num: 121358
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.951A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1397A>G
  hgvsp: ENSP00000440556.1:p.Asn466Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1397A>G
  hgvsp: ENSP00000363296.3:p.Asn466Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.890A>G
  hgvsp: ENSP00000437730.1:p.Asn297Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.998A>G
  hgvsp: ENSP00000477466.1:p.Asn333Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.977A>G
  hgvsp: ENSP00000398456.2:p.Asn326Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.998A>G
  hgvsp: ENSP00000437925.1:p.Asn333Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1872A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*634A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1049A>G
  hgvsp: ENSP00000363292.3:p.Asn350Ser
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6185
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn466Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD

6-34008069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008069
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008069
    reference: chr 6
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1392C>T
  hgvsp: ENST00000374181.4:c.1392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.993C>T
  hgvsp: ENST00000535756.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1044C>T
  hgvsp: ENST00000374177.3:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.885C>T
  hgvsp: ENST00000544773.2:c.885C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*629C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1867C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.993C>T
  hgvsp: ENST00000609222.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1392C>T
  hgvsp: ENST00000538487.2:c.1392C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.946C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.972C>T
  hgvsp: ENST00000455714.2:c.972C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr464Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

6-34008070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008070
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008070
    reference: chr 6
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.992C>T
  hgvsp: ENSP00000477466.1:p.Thr331Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1866C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.945C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.971C>T
  hgvsp: ENSP00000398456.2:p.Thr324Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1043C>T
  hgvsp: ENSP00000363292.3:p.Thr348Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.992C>T
  hgvsp: ENSP00000437925.1:p.Thr331Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1391C>T
  hgvsp: ENSP00000440556.1:p.Thr464Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.884C>T
  hgvsp: ENSP00000437730.1:p.Thr295Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*628C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1391C>T
  hgvsp: ENSP00000363296.3:p.Thr464Ile
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr464Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

http://identifiers.org/exac.variant/6-34008086-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008086
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008086
    reference: chr 6
allele count: 2
allele frequency: 1.649620587264929e-5
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*612G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.868G>T
  hgvsp: ENSP00000437730.1:p.Ala290Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.976G>T
  hgvsp: ENSP00000477466.1:p.Ala326Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1375G>T
  hgvsp: ENSP00000363296.3:p.Ala459Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.976G>T
  hgvsp: ENSP00000437925.1:p.Ala326Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.929G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1027G>T
  hgvsp: ENSP00000363292.3:p.Ala343Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.955G>T
  hgvsp: ENSP00000398456.2:p.Ala319Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1850G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1375G>T
  hgvsp: ENSP00000440556.1:p.Ala459Ser
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala459Ser
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: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD

6-34008087-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008087
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008087
    reference: chr 6
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1374C>T
  hgvsp: ENST00000374181.4:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.975C>T
  hgvsp: ENST00000535756.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.975C>T
  hgvsp: ENST00000609222.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.867C>T
  hgvsp: ENST00000544773.2:c.867C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1374C>T
  hgvsp: ENST00000538487.2:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*611C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1849C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.928C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.954C>T
  hgvsp: ENST00000455714.2:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1026C>T
  hgvsp: ENST00000374177.3:c.1026C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4025
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1505
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile458Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

6-34008089-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008089
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008088
    reference: chr 6
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.925delC
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.972delC
  hgvsp: ENSP00000437925.1:p.Ile325SerfsTer6
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*608delC
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.864delC
  hgvsp: ENSP00000437730.1:p.Ile289SerfsTer6
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.951delC
  hgvsp: ENSP00000398456.2:p.Ile318SerfsTer6
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1371delC
  hgvsp: ENSP00000363296.3:p.Ile458SerfsTer6
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1023delC
  hgvsp: ENSP00000363292.3:p.Ile342SerfsTer6
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1846delC
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.972delC
  hgvsp: ENSP00000477466.1:p.Ile325SerfsTer6
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1371delC
  hgvsp: ENSP00000440556.1:p.Ile458SerfsTer6
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2998
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile458SerfsTer6
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: TG
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-34008094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008094
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008094
    reference: chr 6
allele count: 2
allele frequency: 1.651227687785869e-5
allele num: 121122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-3C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-3C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1370-3C>T
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-34008099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008099
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008099
    reference: chr 6
allele count: 2
allele frequency: 1.652264428399121e-5
allele num: 121046
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-8C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-8C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5982
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1370-8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/6-34008105-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008105
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008105
    reference: chr 6
allele count: 2
allele frequency: 1.653521173338625e-5
allele num: 120954
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-14G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-14G>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45973
  bin: 9.75e1
  variant carriers: 2
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: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

6-34008105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008105
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008105
    reference: chr 6
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-14G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-14G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2883
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD

6-34008106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008106
    reference: chr 6
allele count: 813
allele frequency: 6.721785861926416e-3
allele num: 120950
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-15C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-15C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6026
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 7.75e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 8.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 9.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 6.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 9.75e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 8.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 3606
  bin: 7.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 10
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

6-34008117-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008117
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008117
    reference: chr 6
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-26G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-26G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6077
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-34008135-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008135
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008135
    reference: chr 6
allele count: 3
allele frequency: 2.488304966656714e-5
allele num: 120564
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-44C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-44C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3600
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3724
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

6-34008136-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008136
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008136
    reference: chr 6
allele count: 10
allele frequency: 8.302062232258493e-5
allele num: 120452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-45G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-45G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4440
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 8.75e1
  variant carriers: 0
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: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

6-34008140-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008140
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008140
    reference: chr 6
allele count: 5
allele frequency: 4.150893272232185e-5
allele num: 120456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-49C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-49C>G
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1839
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

6-34008142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008142
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008142
    reference: chr 6
allele count: 2
allele frequency: 1.662013030182157e-5
allele num: 120336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1845-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1370-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.863-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.950-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.924-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.971-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1370-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.971-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*607-51C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1022-51C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

6-34008283-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008283
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008283
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 81830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+42G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+42G>C
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20336
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16426
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9079
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/6-34008292-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008292
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008292
    reference: chr 6
allele count: 3
allele frequency: 3.615328994938539e-5
allele num: 82980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+33G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+33G>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16526
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19696
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7350
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5243
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

6-34008308-C-CCGCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008308
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008312
    reference: chr 6
allele count: 1
allele frequency: 1.136751165169944e-5
allele num: 87970
alternate allele: CCGCA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+13_970+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+13_1844+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+13_1369+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+13_923+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+13_970+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+13_949+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+13_*606+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+13_1021+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+13_862+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+13_1369+16dupTGCG
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5156
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15363
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

6-34008309-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008309
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008309
    reference: chr 6
allele count: 13
allele frequency: 1.472253680634202e-4
allele num: 88300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+16G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+16G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4966
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15635
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17651
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/6-34008313-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008313
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008313
    reference: chr 6
allele count: 1
allele frequency: 1.099190995427365e-5
allele num: 90976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+12G>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+12G>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13907
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/6-34008315-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008315
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008315
    reference: chr 6
allele count: 4
allele frequency: 4.344803614876608e-5
allele num: 92064
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+10T>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+10T>G
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19756
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13185
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13914
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20378
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

6-34008321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008321
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008321
    reference: chr 6
allele count: 2
allele frequency: 2.111754022891414e-5
allele num: 94708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+4G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+4G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22004
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1369+4G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-34008322-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008322
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008322
    reference: chr 6
allele count: 1
allele frequency: 1.050221596756916e-5
allele num: 95218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.970+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.949+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.923+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.970+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1369+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1021+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1844+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*606+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.862+3G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1369+3G>C
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 8.25e1
  variant carriers: 0
hgvs: c.1369+3G>C
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

6-34008333-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008333
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008333
    reference: chr 6
allele count: 1
allele frequency: 9.812964889211626e-6
allele num: 101906
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.962A>G
  hgvsp: ENSP00000437925.1:p.Asn321Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1361A>G
  hgvsp: ENSP00000440556.1:p.Asn454Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*598A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1013A>G
  hgvsp: ENSP00000363292.3:p.Asn338Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.915A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1836A>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.941A>G
  hgvsp: ENSP00000398456.2:p.Asn314Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.854A>G
  hgvsp: ENSP00000437730.1:p.Asn285Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1361A>G
  hgvsp: ENSP00000363296.3:p.Asn454Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.962A>G
  hgvsp: ENSP00000477466.1:p.Asn321Ser
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7609
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6938
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn454Ser
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

6-34008337-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008337
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008337
    reference: chr 6
allele count: 1
allele frequency: 9.644131545954286e-6
allele num: 103690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.937G>A
  hgvsp: ENSP00000398456.2:p.Val313Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1357G>A
  hgvsp: ENSP00000363296.3:p.Val453Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1832G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.911G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1009G>A
  hgvsp: ENSP00000363292.3:p.Val337Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*594G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.958G>A
  hgvsp: ENSP00000437925.1:p.Val320Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.958G>A
  hgvsp: ENSP00000477466.1:p.Val320Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.850G>A
  hgvsp: ENSP00000437730.1:p.Val284Ile
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1357G>A
  hgvsp: ENSP00000440556.1:p.Val453Ile
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2336
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10016
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val453Ile
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

6-34008338-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008338
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008338
    reference: chr 6
allele count: 1
allele frequency: 9.571026588311863e-6
allele num: 104482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.910C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.936C>T
  hgvsp: ENST00000455714.2:c.936C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.849C>T
  hgvsp: ENST00000544773.2:c.849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1008C>T
  hgvsp: ENST00000374177.3:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.957C>T
  hgvsp: ENST00000609222.1:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*593C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1356C>T
  hgvsp: ENST00000538487.2:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1831C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1356C>T
  hgvsp: ENST00000374181.4:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.957C>T
  hgvsp: ENST00000535756.1:c.957C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6353
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn452Asn
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-34008342-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008342
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008342
    reference: chr 6
allele count: 1
allele frequency: 9.418856550814731e-6
allele num: 106170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.845G>A
  hgvsp: ENSP00000437730.1:p.Arg282Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.953G>A
  hgvsp: ENSP00000477466.1:p.Arg318Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.906G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1827G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.932G>A
  hgvsp: ENSP00000398456.2:p.Arg311Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.953G>A
  hgvsp: ENSP00000437925.1:p.Arg318Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1004G>A
  hgvsp: ENSP00000363292.3:p.Arg335Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1352G>A
  hgvsp: ENSP00000363296.3:p.Arg451Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1352G>A
  hgvsp: ENSP00000440556.1:p.Arg451Gln
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*589G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1922
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg451Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

6-34008343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008343
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008343
    reference: chr 6
allele count: 1
allele frequency: 9.348939830223253e-6
allele num: 106964
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.931C>T
  hgvsp: ENSP00000398456.2:p.Arg311Ter
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.952C>T
  hgvsp: ENSP00000477466.1:p.Arg318Ter
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1351C>T
  hgvsp: ENSP00000440556.1:p.Arg451Ter
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.844C>T
  hgvsp: ENSP00000437730.1:p.Arg282Ter
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1351C>T
  hgvsp: ENSP00000363296.3:p.Arg451Ter
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.905C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.1003C>T
  hgvsp: ENSP00000363292.3:p.Arg335Ter
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.952C>T
  hgvsp: ENSP00000437925.1:p.Arg318Ter
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1826C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*588C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32379
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg451Ter
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

6-34008376-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008376
    reference: chr 6
allele count: 1
allele frequency: 8.524713143402724e-6
allele num: 117306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.919C>T
  hgvsp: ENSP00000437925.1:p.Pro307Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.898C>T
  hgvsp: ENSP00000398456.2:p.Pro300Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*555C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1318C>T
  hgvsp: ENSP00000363296.3:p.Pro440Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.970C>T
  hgvsp: ENSP00000363292.3:p.Pro324Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.811C>T
  hgvsp: ENSP00000437730.1:p.Pro271Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.872C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.919C>T
  hgvsp: ENSP00000477466.1:p.Pro307Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1793C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1318C>T
  hgvsp: ENSP00000440556.1:p.Pro440Ser
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro440Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

6-34008376-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008376
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008376
    reference: chr 6
allele count: 1
allele frequency: 8.524713143402724e-6
allele num: 117306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.898C>G
  hgvsp: ENSP00000398456.2:p.Pro300Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.919C>G
  hgvsp: ENSP00000437925.1:p.Pro307Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.872C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.970C>G
  hgvsp: ENSP00000363292.3:p.Pro324Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1793C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.919C>G
  hgvsp: ENSP00000477466.1:p.Pro307Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.811C>G
  hgvsp: ENSP00000437730.1:p.Pro271Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1318C>G
  hgvsp: ENSP00000440556.1:p.Pro440Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*555C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1318C>G
  hgvsp: ENSP00000363296.3:p.Pro440Ala
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5697
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro440Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

6-34008377-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008377
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008377
    reference: chr 6
allele count: 1
allele frequency: 8.517307168165713e-6
allele num: 117408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1317C>G
  hgvsp: ENSP00000363296.3:p.Asp439Glu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.918C>G
  hgvsp: ENSP00000437925.1:p.Asp306Glu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.871C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.810C>G
  hgvsp: ENSP00000437730.1:p.Asp270Glu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1792C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.897C>G
  hgvsp: ENSP00000398456.2:p.Asp299Glu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*554C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1317C>G
  hgvsp: ENSP00000440556.1:p.Asp439Glu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.918C>G
  hgvsp: ENSP00000477466.1:p.Asp306Glu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.969C>G
  hgvsp: ENSP00000363292.3:p.Asp323Glu
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12328
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp439Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum

6-34008382-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008382
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008382
    reference: chr 6
allele count: 3
allele frequency: 2.540263171264543e-5
allele num: 118098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.866A>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*549A>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.913A>C
  hgvsp: ENSP00000437925.1:p.Met305Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1312A>C
  hgvsp: ENSP00000363296.3:p.Met438Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1312A>C
  hgvsp: ENSP00000440556.1:p.Met438Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.805A>C
  hgvsp: ENSP00000437730.1:p.Met269Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.913A>C
  hgvsp: ENSP00000477466.1:p.Met305Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.892A>C
  hgvsp: ENSP00000398456.2:p.Met298Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1787A>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.964A>C
  hgvsp: ENSP00000363292.3:p.Met322Leu
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37477
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12830
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Met438Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

6-34008383-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008383
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008383
    reference: chr 6
allele count: 1
allele frequency: 8.456230550669733e-6
allele num: 118256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.891C>T
  hgvsp: ENST00000455714.2:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*548C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.912C>T
  hgvsp: ENST00000609222.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.804C>T
  hgvsp: ENST00000544773.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.963C>T
  hgvsp: ENST00000374177.3:c.963C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1311C>T
  hgvsp: ENST00000538487.2:c.1311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.912C>T
  hgvsp: ENST00000535756.1:c.912C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1311C>T
  hgvsp: ENST00000374181.4:c.1311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1786C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.865C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg437Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-34008384-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008384
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008384
    reference: chr 6
allele count: 2
allele frequency: 1.690588493854711e-5
allele num: 118302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.803G>C
  hgvsp: ENSP00000437730.1:p.Arg268Pro
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.911G>C
  hgvsp: ENSP00000437925.1:p.Arg304Pro
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1785G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1310G>C
  hgvsp: ENSP00000440556.1:p.Arg437Pro
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*547G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.911G>C
  hgvsp: ENSP00000477466.1:p.Arg304Pro
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.890G>C
  hgvsp: ENSP00000398456.2:p.Arg297Pro
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.864G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.962G>C
  hgvsp: ENSP00000363292.3:p.Arg321Pro
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1310G>C
  hgvsp: ENSP00000363296.3:p.Arg437Pro
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37263
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5863
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg437Pro
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

6-34008384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008384
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008384
    reference: chr 6
allele count: 5
allele frequency: 4.226471234636777e-5
allele num: 118302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1785G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.803G>A
  hgvsp: ENSP00000437730.1:p.Arg268His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.890G>A
  hgvsp: ENSP00000398456.2:p.Arg297His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.864G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1310G>A
  hgvsp: ENSP00000440556.1:p.Arg437His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.911G>A
  hgvsp: ENSP00000477466.1:p.Arg304His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1310G>A
  hgvsp: ENSP00000363296.3:p.Arg437His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.911G>A
  hgvsp: ENSP00000437925.1:p.Arg304His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.962G>A
  hgvsp: ENSP00000363292.3:p.Arg321His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*547G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13071
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg437His
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: C
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

6-34008385-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008385
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008385
    reference: chr 6
allele count: 1
allele frequency: 8.424741781664392e-6
allele num: 118698
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.910C>T
  hgvsp: ENSP00000437925.1:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1309C>T
  hgvsp: ENSP00000440556.1:p.Arg437Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*546C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.889C>T
  hgvsp: ENSP00000398456.2:p.Arg297Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.802C>T
  hgvsp: ENSP00000437730.1:p.Arg268Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1309C>T
  hgvsp: ENSP00000363296.3:p.Arg437Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.863C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.910C>T
  hgvsp: ENSP00000477466.1:p.Arg304Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.961C>T
  hgvsp: ENSP00000363292.3:p.Arg321Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1784C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg437Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-34008386-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008386
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008386
    reference: chr 6
allele count: 2
allele frequency: 1.683189981653229e-5
allele num: 118822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.909G>C
  hgvsp: ENST00000535756.1:c.909G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.909G>C
  hgvsp: ENST00000609222.1:c.909G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.888G>C
  hgvsp: ENST00000455714.2:c.888G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.801G>C
  hgvsp: ENST00000544773.2:c.801G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*545G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1308G>C
  hgvsp: ENST00000374181.4:c.1308G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1783G>C
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1308G>C
  hgvsp: ENST00000538487.2:c.1308G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.960G>C
  hgvsp: ENST00000374177.3:c.960G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.862G>C
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13377
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro436Pro
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

6-34008386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008386
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008386
    reference: chr 6
allele count: 14
allele frequency: 1.178232987157261e-4
allele num: 118822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.888G>A
  hgvsp: ENST00000455714.2:c.888G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.909G>A
  hgvsp: ENST00000535756.1:c.909G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.909G>A
  hgvsp: ENST00000609222.1:c.909G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.862G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1783G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*545G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1308G>A
  hgvsp: ENST00000374181.4:c.1308G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.960G>A
  hgvsp: ENST00000374177.3:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1308G>A
  hgvsp: ENST00000538487.2:c.1308G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.801G>A
  hgvsp: ENST00000544773.2:c.801G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13377
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37303
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro436Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

6-34008387-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008387
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008387
    reference: chr 6
allele count: 4
allele frequency: 3.360215053763441e-5
allele num: 119040
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.800C>T
  hgvsp: ENSP00000437730.1:p.Pro267Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1307C>T
  hgvsp: ENSP00000440556.1:p.Pro436Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.861C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1782C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.887C>T
  hgvsp: ENSP00000398456.2:p.Pro296Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.908C>T
  hgvsp: ENSP00000437925.1:p.Pro303Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.908C>T
  hgvsp: ENSP00000477466.1:p.Pro303Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*544C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1307C>T
  hgvsp: ENSP00000363296.3:p.Pro436Leu
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.959C>T
  hgvsp: ENSP00000363292.3:p.Pro320Leu
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro436Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

6-34008394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008394
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008394
    reference: chr 6
allele count: 1
allele frequency: 8.344877079960612e-6
allele num: 119834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1300C>T
  hgvsp: ENSP00000363296.3:p.Leu434Phe
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.854C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1775C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*537C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.793C>T
  hgvsp: ENSP00000437730.1:p.Leu265Phe
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.880C>T
  hgvsp: ENSP00000398456.2:p.Leu294Phe
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1300C>T
  hgvsp: ENSP00000440556.1:p.Leu434Phe
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.901C>T
  hgvsp: ENSP00000437925.1:p.Leu301Phe
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.901C>T
  hgvsp: ENSP00000477466.1:p.Leu301Phe
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.952C>T
  hgvsp: ENSP00000363292.3:p.Leu318Phe
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2089
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu434Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS

6-34008395-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008395
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008395
    reference: chr 6
allele count: 1
allele frequency: 8.343345347750633e-6
allele num: 119856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*536G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.951G>A
  hgvsp: ENST00000374177.3:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.900G>A
  hgvsp: ENST00000609222.1:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.792G>A
  hgvsp: ENST00000544773.2:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1299G>A
  hgvsp: ENST00000538487.2:c.1299G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.879G>A
  hgvsp: ENST00000455714.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1299G>A
  hgvsp: ENST00000374181.4:c.1299G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.853G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1774G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.900G>A
  hgvsp: ENST00000535756.1:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2036
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly433Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

6-34008400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008400
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008400
    reference: chr 6
allele count: 4
allele frequency: 3.329726130025805e-5
allele num: 120130
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1294G>A
  hgvsp: ENSP00000440556.1:p.Val432Met
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.946G>A
  hgvsp: ENSP00000363292.3:p.Val316Met
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.848G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.874G>A
  hgvsp: ENSP00000398456.2:p.Val292Met
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1294G>A
  hgvsp: ENSP00000363296.3:p.Val432Met
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.895G>A
  hgvsp: ENSP00000477466.1:p.Val299Met
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.787G>A
  hgvsp: ENSP00000437730.1:p.Val263Met
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*531G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.895G>A
  hgvsp: ENSP00000437925.1:p.Val299Met
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1769G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val432Met
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

6-34008401-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008401
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008401
    reference: chr 6
allele count: 1
allele frequency: 8.315731701232391e-6
allele num: 120254
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1293C>T
  hgvsp: ENST00000538487.2:c.1293C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1293C>T
  hgvsp: ENST00000374181.4:c.1293C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.873C>T
  hgvsp: ENST00000455714.2:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.786C>T
  hgvsp: ENST00000544773.2:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.894C>T
  hgvsp: ENST00000609222.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.945C>T
  hgvsp: ENST00000374177.3:c.945C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.847C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1768C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*530C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.894C>T
  hgvsp: ENST00000535756.1:c.894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg431Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

6-34008402-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008402
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008402
    reference: chr 6
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1292G>A
  hgvsp: ENSP00000363296.3:p.Arg431His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.846G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.893G>A
  hgvsp: ENSP00000437925.1:p.Arg298His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.785G>A
  hgvsp: ENSP00000437730.1:p.Arg262His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.944G>A
  hgvsp: ENSP00000363292.3:p.Arg315His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1292G>A
  hgvsp: ENSP00000440556.1:p.Arg431His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.893G>A
  hgvsp: ENSP00000477466.1:p.Arg298His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1767G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.872G>A
  hgvsp: ENSP00000398456.2:p.Arg291His
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*529G>A
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg431His
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

6-34008403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008403
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008403
    reference: chr 6
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*528C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.943C>T
  hgvsp: ENSP00000363292.3:p.Arg315Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.871C>T
  hgvsp: ENSP00000398456.2:p.Arg291Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1766C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.784C>T
  hgvsp: ENSP00000437730.1:p.Arg262Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.892C>T
  hgvsp: ENSP00000477466.1:p.Arg298Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1291C>T
  hgvsp: ENSP00000440556.1:p.Arg431Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.845C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1291C>T
  hgvsp: ENSP00000363296.3:p.Arg431Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.892C>T
  hgvsp: ENSP00000437925.1:p.Arg298Cys
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg431Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

6-34008406-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008406
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008406
    reference: chr 6
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.842G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.940G>A
  hgvsp: ENSP00000363292.3:p.Gly314Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1288G>A
  hgvsp: ENSP00000440556.1:p.Gly430Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.868G>A
  hgvsp: ENSP00000398456.2:p.Gly290Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1763G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1288G>A
  hgvsp: ENSP00000363296.3:p.Gly430Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*525G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.781G>A
  hgvsp: ENSP00000437730.1:p.Gly261Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.889G>A
  hgvsp: ENSP00000437925.1:p.Gly297Ser
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.889G>A
  hgvsp: ENSP00000477466.1:p.Gly297Ser
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly430Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

6-34008407-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008407
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008407
    reference: chr 6
allele count: 6
allele frequency: 4.973062577704103e-5
allele num: 120650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.780C>T
  hgvsp: ENST00000544773.2:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.888C>T
  hgvsp: ENST00000609222.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.939C>T
  hgvsp: ENST00000374177.3:c.939C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1762C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1287C>T
  hgvsp: ENST00000374181.4:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1287C>T
  hgvsp: ENST00000538487.2:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.841C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.888C>T
  hgvsp: ENST00000535756.1:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.867C>T
  hgvsp: ENST00000455714.2:c.867C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*524C>T
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro429Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

6-34008409-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008409
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008409
    reference: chr 6
allele count: 6
allele frequency: 4.968450340338848e-5
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.839C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1285C>G
  hgvsp: ENSP00000440556.1:p.Pro429Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.886C>G
  hgvsp: ENSP00000477466.1:p.Pro296Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.778C>G
  hgvsp: ENSP00000437730.1:p.Pro260Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1760C>G
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1285C>G
  hgvsp: ENSP00000363296.3:p.Pro429Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.937C>G
  hgvsp: ENSP00000363292.3:p.Pro313Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.865C>G
  hgvsp: ENSP00000398456.2:p.Pro289Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.886C>G
  hgvsp: ENSP00000437925.1:p.Pro296Ala
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*522C>G
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro429Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

6-34008421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008421
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008421
    reference: chr 6
allele count: 5
allele frequency: 4.132572939912389e-5
allele num: 120990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.925C>T
  hgvsp: ENSP00000363292.3:p.Arg309Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.827C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*510C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.766C>T
  hgvsp: ENSP00000437730.1:p.Arg256Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.874C>T
  hgvsp: ENSP00000437925.1:p.Arg292Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1273C>T
  hgvsp: ENSP00000363296.3:p.Arg425Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1748C>T
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.853C>T
  hgvsp: ENSP00000398456.2:p.Arg285Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1273C>T
  hgvsp: ENSP00000440556.1:p.Arg425Cys
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.874C>T
  hgvsp: ENSP00000477466.1:p.Arg292Cys
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Arg425Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-34008430-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 34008430
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 34008430
    reference: chr 6
allele count: 12
allele frequency: 9.911457645037664e-5
allele num: 121072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477016
  ensembl transcript: ENST00000609278
  gene symbol: GRM4
  hgvsc: ENST00000609278.1:c.*501G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363296
  ensembl transcript: ENST00000374181
  gene symbol: GRM4
  hgvsc: ENST00000374181.4:c.1264G>A
  hgvsp: ENSP00000363296.3:p.Ala422Thr
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000363292
  ensembl transcript: ENST00000374177
  gene symbol: GRM4
  hgvsc: ENST00000374177.3:c.916G>A
  hgvsp: ENSP00000363292.3:p.Ala306Thr
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000477466
  ensembl transcript: ENST00000609222
  gene symbol: GRM4
  hgvsc: ENST00000609222.1:c.865G>A
  hgvsp: ENSP00000477466.1:p.Ala289Thr
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437730
  ensembl transcript: ENST00000544773
  gene symbol: GRM4
  hgvsc: ENST00000544773.2:c.757G>A
  hgvsp: ENSP00000437730.1:p.Ala253Thr
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000437925
  ensembl transcript: ENST00000535756
  gene symbol: GRM4
  hgvsc: ENST00000535756.1:c.865G>A
  hgvsp: ENSP00000437925.1:p.Ala289Thr
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000440556
  ensembl transcript: ENST00000538487
  gene symbol: GRM4
  hgvsc: ENST00000538487.2:c.1264G>A
  hgvsp: ENSP00000440556.1:p.Ala422Thr
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000609860
  gene symbol: GRM4
  hgvsc: ENST00000609860.1:n.1739G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000124493
  ensembl transcript: ENST00000545715
  gene symbol: GRM4
  hgvsc: ENST00000545715.1:n.818G>A
  variant of: http://identifiers.org/hgnc/4596
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000124493
  ensembl protein: ENSP00000398456
  ensembl transcript: ENST00000455714
  gene symbol: GRM4
  hgvsc: ENST00000455714.2:c.844G>A
  hgvsp: ENSP00000398456.2:p.Ala282Thr
  variant of: http://identifiers.org/hgnc/4596
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala422Thr
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 633
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48968
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5439
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.177e0

QD
type: SiteQuality
SIO_000300: 1.214e1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.21e0

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 4.605498e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 48982
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1037
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1623
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1038
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
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: 66686
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.607111e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.564e1

VQSLOD
type: SiteQuality
SIO_000300: -9.092e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e0

MQ
type: SiteQuality
SIO_000300: 5.989e1

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

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

GenotypeQuality
all individuals: 769
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1031
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5479
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1042
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48989
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 642
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.978e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.92e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.116e0

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 4.60865e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 2.804e1

GenotypeQuality
all individuals: 21
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5481
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1626
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48994
bin: 9.75e1
variant carriers: 1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.94e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

VQSLOD
type: SiteQuality
SIO_000300: -4.763e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.2525e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e0

DP
type: SiteQuality
SIO_000300: 4.609215e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.784e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5489
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48994
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 1626
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
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: 6614
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 2.57e-1

FS
type: SiteQuality
SIO_000300: 1.3272e1

DP
type: SiteQuality
SIO_000300: 4.6094e6

VQSLOD
type: SiteQuality
SIO_000300: -1.989e0

QD
type: SiteQuality
SIO_000300: 2.642e1

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

GenotypeQuality
all individuals: 5489
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48996
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1047
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.28e-1

QD
type: SiteQuality
SIO_000300: 1.122e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e0

DP
type: SiteQuality
SIO_000300: 4.609627e6

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

GenotypeQuality
all individuals: 932
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 835
bin: 9.25e1
variant carriers: 18

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3475
bin: 6.25e1
variant carriers: 6

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 429
bin: 7.25e1
variant carriers: 4

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 53165
bin: 9.75e1
variant carriers: 30859

GenotypeQuality
all individuals: 459
bin: 8.75e1
variant carriers: 7

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 6

GenotypeQuality
all individuals: 640
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 1

African
type: Population
allele count: 7467
allele frequency: 7.177047289504037e-1
allele num: 10404
num of homozygotes: 2695

South Asian
type: Population
allele count: 4677
allele frequency: 2.8328285887341e-1
allele num: 16510
num of homozygotes: 701

Other
type: Population
allele count: 274
allele frequency: 3.017621145374449e-1
allele num: 908
num of homozygotes: 41

Latino
type: Population
allele count: 6397
allele frequency: 5.52895419187554e-1
allele num: 11570
num of homozygotes: 1832

East Asian
type: Population
allele count: 4109
allele frequency: 4.769034354688951e-1
allele num: 8616
num of homozygotes: 996

European (Non-Finnish)
type: Population
allele count: 14700
allele frequency: 2.202907238123782e-1
allele num: 66730
num of homozygotes: 1627

European (Finnish)
type: Population
allele count: 1336
allele frequency: 2.020568663036903e-1
allele num: 6612
num of homozygotes: 145

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.245e-1

DP
type: SiteQuality
SIO_000300: 6.506583e6

VQSLOD
type: SiteQuality
SIO_000300: 3.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.967e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6193
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 942
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46043
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.539638e6

QD
type: SiteQuality
SIO_000300: 1.332e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.401e0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

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

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

GenotypeQuality
all individuals: 1511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1953
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46043
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1801
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 869
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variant carriers: 0

GenotypeQuality
all individuals: 942
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.21e-1

QD
type: SiteQuality
SIO_000300: 2.034e1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.727e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.539381e6

GenotypeQuality
all individuals: 1511
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1363
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6201
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 941
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 46042
bin: 9.75e1
variant carriers: 262

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

Latino
type: Population
allele count: 251
allele frequency: 2.167904646743824e-2
allele num: 11578
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.09781826900024e-4
allele num: 66736
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: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.93e-2

QD
type: SiteQuality
SIO_000300: 1.46e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.35e0

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.541296e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e-1

GenotypeQuality
all individuals: 45993
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 948
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variant carriers: 0

GenotypeQuality
all individuals: 6211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 873
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 1372
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1813
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e0

FS
type: SiteQuality
SIO_000300: 5.048e0

DP
type: SiteQuality
SIO_000300: 3.513887e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.158e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.627e0

QD
type: SiteQuality
SIO_000300: 8.99e0

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

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 6217
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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European (Non-Finnish)
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South Asian
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European (Finnish)
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African
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MQ
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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VQSLOD
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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DP
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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Other
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East Asian
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African
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QD
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FS
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MQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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ClippingRankSum
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QD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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Latino
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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FS
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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Latino
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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DP
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InbreedingCoeff
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MQ
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FS
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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Latino
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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FS
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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InbreedingCoeff
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DP
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QD
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MQ
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FS
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele frequency: 2.998320940273447e-5
allele num: 66704
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele num: 908
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -1.48e-1

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66704
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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East Asian
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allele frequency: 1.155535012710885e-4
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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QD
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

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

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

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

European (Finnish)
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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QD
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
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ClippingRankSum
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FS
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MQ
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SIO_000300: 5.963e1

DP
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ReadPosRankSum
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SIO_000300: -6.16e-1

BaseQRankSum
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SIO_000300: -4.25e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele num: 66660
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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MQ
type: SiteQuality
SIO_000300: 6.049e1

FS
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DP
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10396
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Non-Finnish)
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East Asian
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South Asian
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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MQ
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VQSLOD
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QD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

European (Non-Finnish)
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allele count: 2
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allele num: 66604
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Other
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East Asian
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South Asian
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European (Finnish)
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African
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Latino
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

Other
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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ClippingRankSum
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 2.141e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

DP
type: SiteQuality
SIO_000300: 3.494455e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.982e1

QD
type: SiteQuality
SIO_000300: 1.033e1

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
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GenotypeQuality
all individuals: 1802
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variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

FS
type: SiteQuality
SIO_000300: 2.141e0

MQRankSum
type: SiteQuality
SIO_000300: -5.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 3.494455e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.102e0

QD
type: SiteQuality
SIO_000300: 1.033e1

GenotypeQuality
all individuals: 813
bin: 7.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 801

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1309
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variant carriers: 1

GenotypeQuality
all individuals: 1474
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variant carriers: 0

South Asian
type: Population
allele count: 40
allele frequency: 2.462144527883787e-3
allele num: 16246
num of homozygotes: 2

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: 340
allele frequency: 5.107252298263534e-3
allele num: 66572
num of homozygotes: 3

Other
type: Population
allele count: 7
allele frequency: 7.743362831858407e-3
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 325
allele frequency: 3.128609934539853e-2
allele num: 10388
num of homozygotes: 4

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

Latino
type: Population
allele count: 100
allele frequency: 8.637070305752288e-3
allele num: 11578
num of homozygotes: 1

VQSLOD
type: SiteQuality
SIO_000300: 5.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.08e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

DP
type: SiteQuality
SIO_000300: 3.489136e6

MQ
type: SiteQuality
SIO_000300: 5.975e1

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

GenotypeQuality
all individuals: 4491
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1523
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variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.553e0

DP
type: SiteQuality
SIO_000300: 3.447875e6

QD
type: SiteQuality
SIO_000300: 7.8e0

MQRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.784e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.75e0

FS
type: SiteQuality
SIO_000300: 4.824e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45816
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 878
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GenotypeQuality
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GenotypeQuality
all individuals: 60
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GenotypeQuality
all individuals: 860
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 748
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variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.876407305479109e-4
allele num: 15988
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.71e-1

FS
type: SiteQuality
SIO_000300: 4.007e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.672e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.595e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 3.427009e6

GenotypeQuality
all individuals: 1824
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
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variant carriers: 0

GenotypeQuality
all individuals: 863
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variant carriers: 0

GenotypeQuality
all individuals: 34
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GenotypeQuality
all individuals: 1231
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GenotypeQuality
all individuals: 94
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GenotypeQuality
all individuals: 850
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GenotypeQuality
all individuals: 66
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GenotypeQuality
all individuals: 2358
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 563
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GenotypeQuality
all individuals: 428
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variant carriers: 0

GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 45816
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 916
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variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 6.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15900
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.505072092953252e-4
allele num: 66442
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.325e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

QD
type: SiteQuality
SIO_000300: 1.268e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
SIO_000300: 3.426286e6

GenotypeQuality
all individuals: 947
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
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variant carriers: 0

GenotypeQuality
all individuals: 802
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variant carriers: 0

GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 891
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 736
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GenotypeQuality
all individuals: 1225
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GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
all individuals: 466
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GenotypeQuality
all individuals: 944
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GenotypeQuality
all individuals: 45815
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variant carriers: 5

GenotypeQuality
all individuals: 2008
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variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 5.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 5
allele frequency: 3.14228255404726e-4
allele num: 15912
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.23e1

DP
type: SiteQuality
SIO_000300: 3.423336e6

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.082e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.447e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 889
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 569
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GenotypeQuality
all individuals: 1214
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GenotypeQuality
all individuals: 68
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GenotypeQuality
all individuals: 725
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GenotypeQuality
all individuals: 946
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GenotypeQuality
all individuals: 45808
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
all individuals: 168
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GenotypeQuality
all individuals: 844
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GenotypeQuality
all individuals: 783
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GenotypeQuality
all individuals: 1824
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GenotypeQuality
all individuals: 1718
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GenotypeQuality
all individuals: 1194
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variant carriers: 0

GenotypeQuality
all individuals: 1458
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505570611261668e-5
allele num: 66420
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15812
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
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: 10384
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.578e-1

QD
type: SiteQuality
SIO_000300: 1.558e1

MQRankSum
type: SiteQuality
SIO_000300: -3.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.48e0

DP
type: SiteQuality
SIO_000300: 3.422182e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

FS
type: SiteQuality
SIO_000300: 1.0092e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2374
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8439
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GenotypeQuality
all individuals: 1128
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GenotypeQuality
all individuals: 2481
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GenotypeQuality
all individuals: 1028
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 291
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GenotypeQuality
all individuals: 2619
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GenotypeQuality
all individuals: 5709
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 268
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7044
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 9.45218e5

GenotypeQuality
all individuals: 584
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1668
bin: 4.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5072
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4270
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7140
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.112932013629726e-5
allele num: 12326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.320400933206602e-5
allele num: 46292
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.272e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.53e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

FS
type: SiteQuality
SIO_000300: 1.235e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.75182e5

GenotypeQuality
all individuals: 3783
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 825
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12956
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.80635838150289e-4
allele num: 5536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48964
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.890000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.582e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.063948e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 13

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 541
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variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7522
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 9.208103130755065e-4
allele num: 13032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.035830618892508e-5
allele num: 49120
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

FS
type: SiteQuality
SIO_000300: 1.519e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.71e-1

DP
type: SiteQuality
SIO_000300: 1.075097e6

QD
type: SiteQuality
SIO_000300: 1.401e1

GenotypeQuality
all individuals: 1049
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18447
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3067
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variant carriers: 0

GenotypeQuality
all individuals: 16693
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.975347661188369e-5
allele num: 50624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7660
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13330
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQRankSum
type: SiteQuality
SIO_000300: -1.922e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

DP
type: SiteQuality
SIO_000300: 1.116414e6

VQSLOD
type: SiteQuality
SIO_000300: -2.425e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.238e1

MQ
type: SiteQuality
SIO_000300: 5.886e1

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2630
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.8064012490242e-5
allele num: 51240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4680
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13444
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.074e0

DP
type: SiteQuality
SIO_000300: 1.131616e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-1

QD
type: SiteQuality
SIO_000300: 9.58e0

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

GenotypeQuality
all individuals: 895
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 236
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.152604887044721e-4
allele num: 8676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4818
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.267441860465116e-5
allele num: 13760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52630
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.174152e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
SIO_000300: 3.31e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

FS
type: SiteQuality
SIO_000300: 8.416e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.743e0

MQRankSum
type: SiteQuality
SIO_000300: 7.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.109e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4828
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.2531328320802e-4
allele num: 7980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52912
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13784
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.461e0

DP
type: SiteQuality
SIO_000300: 1.181115e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.427e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQ
type: SiteQuality
SIO_000300: 5.878e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.024e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.292e1

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 259
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GenotypeQuality
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GenotypeQuality
all individuals: 688
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GenotypeQuality
all individuals: 154
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.767783906095319e-5
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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East Asian
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.737679849864461e-5
allele num: 57548
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South Asian
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ClippingRankSum
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele num: 9806
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.699986400108799e-5
allele num: 58824
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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VQSLOD
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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South Asian
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East Asian
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allele num: 7440
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African
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
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MQ
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BaseQRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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African
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Other
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MQRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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African
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South Asian
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European (Non-Finnish)
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European (Finnish)
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QD
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FS
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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Other
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African
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East Asian
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South Asian
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Latino
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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VQSLOD
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QD
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.864048713806387e-4
allele num: 16094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65082
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.337e1

MQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

DP
type: SiteQuality
SIO_000300: 1.524616e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

FS
type: SiteQuality
SIO_000300: 3.404e0

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
all individuals: 5884
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534825183411609e-5
allele num: 65154
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16108
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.76e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.527236e6

FS
type: SiteQuality
SIO_000300: 3.211e0

QD
type: SiteQuality
SIO_000300: 1.295e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.171e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.394e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-2

GenotypeQuality
all individuals: 426
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 429
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variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 1.996007984031936e-4
allele num: 10020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16110
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.292e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.573e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.224e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 1.53224e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

GenotypeQuality
all individuals: 1886
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.13704010555709e-5
allele num: 65178
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10020
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.207324643078833e-5
allele num: 16110
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

FS
type: SiteQuality
SIO_000300: 1.573e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.224e0

QD
type: SiteQuality
SIO_000300: 1.292e1

DP
type: SiteQuality
SIO_000300: 1.53224e6

GenotypeQuality
all individuals: 385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1957
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.75e1
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GenotypeQuality
all individuals: 6017
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variant carriers: 0

GenotypeQuality
all individuals: 2694
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1633
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
all individuals: 1100
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GenotypeQuality
all individuals: 304
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GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
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variant carriers: 0

GenotypeQuality
all individuals: 364
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variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529379377848469e-5
allele num: 65386
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.21e1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

DP
type: SiteQuality
SIO_000300: 1.536025e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65440
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.331545814875262e-4
allele num: 8578
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.43e-1

DP
type: SiteQuality
SIO_000300: 1.539684e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.113e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.176652254478072e-5
allele num: 16190
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.112469437652811e-5
allele num: 65440
num of homozygotes: 0

East Asian
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allele count: 9
allele frequency: 1.049195616693868e-3
allele num: 8578
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.259e1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.84016973125884e-5
allele num: 11312
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.233197681588359e-4
allele num: 16218
num of homozygotes: 0

Other
type: Population
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5253668507276e-5
allele num: 65558
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.918e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.545213e6

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 456
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GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516208266367468e-5
allele num: 65954
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.415e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.64e0

QD
type: SiteQuality
SIO_000300: 1.717e1

VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.557717e6

FS
type: SiteQuality
SIO_000300: 1.3125e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515978412467406e-5
allele num: 65964
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.688e0

BaseQRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 7.185e0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.559005e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-1

MQ
type: SiteQuality
SIO_000300: 5.839e1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.049423792383776e-5
allele num: 66122
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.565089e6

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.218e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.53e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 1.3206e1

VQSLOD
type: SiteQuality
SIO_000300: -1.717e0

QD
type: SiteQuality
SIO_000300: 1.384e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.86e-1

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5109391998066e-5
allele num: 66184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16384
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.566514e6

MQ
type: SiteQuality
SIO_000300: 5.93e1

FS
type: SiteQuality
SIO_000300: 3.812e0

VQSLOD
type: SiteQuality
SIO_000300: 5.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 4.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

GenotypeQuality
all individuals: 7
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variant carriers: 0

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

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: 10236
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510665296996797e-5
allele num: 66196
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e0

QD
type: SiteQuality
SIO_000300: 1.351e1

FS
type: SiteQuality
SIO_000300: 1.448e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.934e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.567962e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.570259e6

MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

South Asian
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allele frequency: 6.087909411907951e-5
allele num: 16426
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East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66350
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.56e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 16436
num of homozygotes: 0

East Asian
type: Population
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Latino
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allele frequency: 1.74246384387524e-4
allele num: 11478
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African
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allele count: 3
allele frequency: 2.9165856503986e-4
allele num: 10286
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506614035616356e-5
allele num: 66374
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Other
type: Population
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allele frequency: 0.0e0
allele num: 900
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DP
type: SiteQuality
SIO_000300: 1.576607e6

MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: 5.76e-1

QD
type: SiteQuality
SIO_000300: 1.467e1

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6509
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2723
bin: 9.75e1
variant carriers: 6

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

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

GenotypeQuality
all individuals: 2150
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 8.25e1
variant carriers: 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: 6552
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.029888932366133e-5
allele num: 66446
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: 6.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

FS
type: SiteQuality
SIO_000300: 4.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.577338e6

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.25e-1

QD
type: SiteQuality
SIO_000300: 1.505e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
all individuals: 288
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44302
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2154
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.010157165609881e-5
allele num: 66554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.94e0

DP
type: SiteQuality
SIO_000300: 1.58256e6

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.402e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1