3-6903285-CAAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903285
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903282
    reference: chr 3
allele count: 1
allele frequency: 1.055208509201418e-5
allele num: 94768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32896_-106+32898delAGA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.212_214delAGA
  hgvsp: ENSP00000373986.3:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.212_214delAGA
  hgvsp: ENSP00000384585.2:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.212_214delAGA
  hgvsp: ENSP00000417536.1:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.212_214delAGA
  hgvsp: ENSP00000419835.1:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.212_214delAGA
  hgvsp: ENSP00000412329.3:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.212_214delAGA
  hgvsp: ENSP00000350348.4:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.212_214delAGA
  hgvsp: ENSP00000373987.4:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22620_*29-22618delAGA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.212_214delAGA
  hgvsp: ENSP00000385664.1:p.Lys71del
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 12665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2996
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys71del
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CAAG
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

3-6903289-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903289
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903289
    reference: chr 3
allele count: 1
allele frequency: 1.029145397661782e-5
allele num: 97168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.214A>G
  hgvsp: ENSP00000417536.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22618A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32898A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.214A>G
  hgvsp: ENSP00000373987.4:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.214A>G
  hgvsp: ENSP00000384585.2:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.214A>G
  hgvsp: ENSP00000385664.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.214A>G
  hgvsp: ENSP00000419835.1:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.214A>G
  hgvsp: ENSP00000412329.3:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.214A>G
  hgvsp: ENSP00000373986.3:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.214A>G
  hgvsp: ENSP00000350348.4:p.Arg72Gly
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2181
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg72Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

3-6903291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903291
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903291
    reference: chr 3
allele count: 1
allele frequency: 1.021429592858164e-5
allele num: 97902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.216G>A
  hgvsp: ENST00000486284.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22616G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.216G>A
  hgvsp: ENST00000389335.3:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.216G>A
  hgvsp: ENST00000440923.3:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.216G>A
  hgvsp: ENST00000357716.4:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.216G>A
  hgvsp: ENST00000402647.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.216G>A
  hgvsp: ENST00000403881.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32900G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.216G>A
  hgvsp: ENST00000389336.4:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.216G>A
  hgvsp: ENST00000467425.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6709
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6613
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg72Arg
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

3-6903297-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903297
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903297
    reference: chr 3
allele count: 46825
allele frequency: 4.178117638660861e-1
allele num: 112072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22610C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.222C>T
  hgvsp: ENST00000389335.3:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.222C>T
  hgvsp: ENST00000357716.4:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32906C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.222C>T
  hgvsp: ENST00000403881.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.222C>T
  hgvsp: ENST00000467425.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.222C>T
  hgvsp: ENST00000402647.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.222C>T
  hgvsp: ENST00000440923.3:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.222C>T
  hgvsp: ENST00000486284.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.222C>T
  hgvsp: ENST00000389336.4:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.75e1
  variant carriers: 888
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 4.25e1
  variant carriers: 1756
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 10183
  bin: 2.75e1
  variant carriers: 6980
genotype depth: GenotypeDepth
  all individuals: 5528
  bin: 3.25e1
  variant carriers: 4672
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 7.5e0
  variant carriers: 755
genotype depth: GenotypeDepth
  all individuals: 20280
  bin: 2.25e1
  variant carriers: 8195
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.75e1
  variant carriers: 135
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 184
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 1.25e1
  variant carriers: 3451
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 3.75e1
  variant carriers: 3040
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 5.25e1
  variant carriers: 529
genotype depth: GenotypeDepth
  all individuals: 8102
  bin: 1.75e1
  variant carriers: 7068
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 2.5e0
  variant carriers: 114
hgvs: p.Asn74Asn
num of homozygotes: 9544
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

3-6903303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903303
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903303
    reference: chr 3
allele count: 19
allele frequency: 1.665293529896401e-4
allele num: 114094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.228C>T
  hgvsp: ENST00000389335.3:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32912C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.228C>T
  hgvsp: ENST00000357716.4:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.228C>T
  hgvsp: ENST00000440923.3:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.228C>T
  hgvsp: ENST00000486284.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.228C>T
  hgvsp: ENST00000403881.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22604C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.228C>T
  hgvsp: ENST00000389336.4:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.228C>T
  hgvsp: ENST00000402647.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.228C>T
  hgvsp: ENST00000467425.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3347
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12480
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21769
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5053
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1988
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile76Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

3-6903306-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903306
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903306
    reference: chr 3
allele count: 1
allele frequency: 8.742787200559538e-6
allele num: 114380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.231C>T
  hgvsp: ENST00000389335.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.231C>T
  hgvsp: ENST00000403881.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.231C>T
  hgvsp: ENST00000486284.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.231C>T
  hgvsp: ENST00000389336.4:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.231C>T
  hgvsp: ENST00000467425.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.231C>T
  hgvsp: ENST00000402647.2:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32915C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.231C>T
  hgvsp: ENST00000357716.4:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.231C>T
  hgvsp: ENST00000440923.3:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22601C>T
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His77His
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-6903308-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903308
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903308
    reference: chr 3
allele count: 1
allele frequency: 8.729812309035356e-6
allele num: 114550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.233G>A
  hgvsp: ENSP00000373986.3:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.233G>A
  hgvsp: ENSP00000350348.4:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.233G>A
  hgvsp: ENSP00000384585.2:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.233G>A
  hgvsp: ENSP00000385664.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.233G>A
  hgvsp: ENSP00000417536.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.233G>A
  hgvsp: ENSP00000373987.4:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32917G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.233G>A
  hgvsp: ENSP00000419835.1:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22599G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.233G>A
  hgvsp: ENSP00000412329.3:p.Arg78Lys
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12694
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg78Lys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

3-6903309-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903309
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903309
    reference: chr 3
allele count: 1
allele frequency: 8.718851901581599e-6
allele num: 114694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.234G>A
  hgvsp: ENST00000440923.3:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.234G>A
  hgvsp: ENST00000467425.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.234G>A
  hgvsp: ENST00000389335.3:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.234G>A
  hgvsp: ENST00000357716.4:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.234G>A
  hgvsp: ENST00000403881.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.234G>A
  hgvsp: ENST00000486284.1:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.234G>A
  hgvsp: ENST00000402647.2:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32918G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.234G>A
  hgvsp: ENST00000389336.4:c.234G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22598G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5162
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg78Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

3-6903315-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903315
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903315
    reference: chr 3
allele count: 1
allele frequency: 8.669568082118148e-6
allele num: 115346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.240A>G
  hgvsp: ENST00000403881.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.240A>G
  hgvsp: ENST00000357716.4:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.240A>G
  hgvsp: ENST00000389336.4:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.240A>G
  hgvsp: ENST00000440923.3:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.240A>G
  hgvsp: ENST00000467425.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.240A>G
  hgvsp: ENST00000486284.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.240A>G
  hgvsp: ENST00000402647.2:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22592A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.240A>G
  hgvsp: ENST00000389335.3:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32924A>G
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23899
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu80Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

3-6903327-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903327
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903327
    reference: chr 3
allele count: 1
allele frequency: 8.610297916307904e-6
allele num: 116140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.252C>T
  hgvsp: ENST00000403881.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.252C>T
  hgvsp: ENST00000467425.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.252C>T
  hgvsp: ENST00000357716.4:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.252C>T
  hgvsp: ENST00000402647.2:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.252C>T
  hgvsp: ENST00000486284.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.252C>T
  hgvsp: ENST00000440923.3:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.252C>T
  hgvsp: ENST00000389336.4:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.252C>T
  hgvsp: ENST00000389335.3:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22580C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32936C>T
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6411
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr84Tyr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

3-6903333-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903333
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903333
    reference: chr 3
allele count: 3
allele frequency: 2.568757064081926e-5
allele num: 116788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.258G>T
  hgvsp: ENST00000402647.2:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.258G>T
  hgvsp: ENST00000403881.1:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.258G>T
  hgvsp: ENST00000467425.1:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32942G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.258G>T
  hgvsp: ENST00000389336.4:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.258G>T
  hgvsp: ENST00000440923.3:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.258G>T
  hgvsp: ENST00000357716.4:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22574G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.258G>T
  hgvsp: ENST00000389335.3:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.258G>T
  hgvsp: ENST00000486284.1:c.258G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14213
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu86Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

3-6903336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903336
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903336
    reference: chr 3
allele count: 1
allele frequency: 8.544379507160189e-6
allele num: 117036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.261C>T
  hgvsp: ENST00000486284.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.261C>T
  hgvsp: ENST00000402647.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.261C>T
  hgvsp: ENST00000389335.3:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.261C>T
  hgvsp: ENST00000467425.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.261C>T
  hgvsp: ENST00000403881.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22571C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32945C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.261C>T
  hgvsp: ENST00000357716.4:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.261C>T
  hgvsp: ENST00000440923.3:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.261C>T
  hgvsp: ENST00000389336.4:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp87Asp
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

3-6903340-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903340
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903340
    reference: chr 3
allele count: 1
allele frequency: 8.520209937972871e-6
allele num: 117368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.265A>G
  hgvsp: ENSP00000412329.3:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.265A>G
  hgvsp: ENSP00000419835.1:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.265A>G
  hgvsp: ENSP00000373986.3:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.265A>G
  hgvsp: ENSP00000417536.1:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.265A>G
  hgvsp: ENSP00000373987.4:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.265A>G
  hgvsp: ENSP00000350348.4:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.265A>G
  hgvsp: ENSP00000385664.1:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.265A>G
  hgvsp: ENSP00000384585.2:p.Ile89Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32949A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22567A>G
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14865
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1338
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile89Val
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-6903346-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903346
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903346
    reference: chr 3
allele count: 10
allele frequency: 8.490550017830156e-5
allele num: 117778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.271A>G
  hgvsp: ENSP00000373987.4:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.271A>G
  hgvsp: ENSP00000385664.1:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.271A>G
  hgvsp: ENSP00000384585.2:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.271A>G
  hgvsp: ENSP00000419835.1:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.271A>G
  hgvsp: ENSP00000412329.3:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22561A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.271A>G
  hgvsp: ENSP00000417536.1:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.271A>G
  hgvsp: ENSP00000350348.4:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.271A>G
  hgvsp: ENSP00000373986.3:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32955A>G
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15182
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27041
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser91Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

3-6903347-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903347
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903347
    reference: chr 3
allele count: 1
allele frequency: 8.487811502682149e-6
allele num: 117816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22560G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.272G>A
  hgvsp: ENSP00000384585.2:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.272G>A
  hgvsp: ENSP00000417536.1:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.272G>A
  hgvsp: ENSP00000412329.3:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.272G>A
  hgvsp: ENSP00000385664.1:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.272G>A
  hgvsp: ENSP00000419835.1:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32956G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.272G>A
  hgvsp: ENSP00000373986.3:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.272G>A
  hgvsp: ENSP00000350348.4:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.272G>A
  hgvsp: ENSP00000373987.4:p.Ser91Asn
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27108
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2756
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser91Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

3-6903358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903358
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903358
    reference: chr 3
allele count: 5
allele frequency: 4.219836607926541e-5
allele num: 118488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.283C>T
  hgvsp: ENST00000440923.3:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.283C>T
  hgvsp: ENST00000389336.4:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.283C>T
  hgvsp: ENST00000486284.1:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.283C>T
  hgvsp: ENST00000403881.1:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32967C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.283C>T
  hgvsp: ENST00000467425.1:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.283C>T
  hgvsp: ENST00000402647.2:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.283C>T
  hgvsp: ENST00000389335.3:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.283C>T
  hgvsp: ENST00000357716.4:c.283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22549C>T
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16110
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2436
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu95Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

3-6903361-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903361
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903361
    reference: chr 3
allele count: 1
allele frequency: 8.425593583067927e-6
allele num: 118686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.286C>T
  hgvsp: ENST00000402647.2:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.286C>T
  hgvsp: ENST00000440923.3:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.286C>T
  hgvsp: ENST00000467425.1:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22546C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.286C>T
  hgvsp: ENST00000486284.1:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.286C>T
  hgvsp: ENST00000389335.3:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.286C>T
  hgvsp: ENST00000389336.4:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.286C>T
  hgvsp: ENST00000403881.1:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32970C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.286C>T
  hgvsp: ENST00000357716.4:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu96Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

3-6903370-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903370
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903370
    reference: chr 3
allele count: 1
allele frequency: 8.385603595746822e-6
allele num: 119252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.295G>A
  hgvsp: ENSP00000419835.1:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.295G>A
  hgvsp: ENSP00000373986.3:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.295G>A
  hgvsp: ENSP00000385664.1:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.295G>A
  hgvsp: ENSP00000373987.4:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22537G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.295G>A
  hgvsp: ENSP00000412329.3:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.295G>A
  hgvsp: ENSP00000417536.1:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.295G>A
  hgvsp: ENSP00000350348.4:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.295G>A
  hgvsp: ENSP00000384585.2:p.Val99Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32979G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27717
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6865
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val99Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

3-6903374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903374
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903374
    reference: chr 3
allele count: 1
allele frequency: 8.372124175345769e-6
allele num: 119444
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.299C>T
  hgvsp: ENSP00000385664.1:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.299C>T
  hgvsp: ENSP00000373987.4:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.299C>T
  hgvsp: ENSP00000412329.3:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.299C>T
  hgvsp: ENSP00000419835.1:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.299C>T
  hgvsp: ENSP00000384585.2:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.299C>T
  hgvsp: ENSP00000350348.4:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.299C>T
  hgvsp: ENSP00000417536.1:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32983C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22533C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.299C>T
  hgvsp: ENSP00000373986.3:p.Thr100Met
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr100Met
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

3-6903375-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903375
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903375
    reference: chr 3
allele count: 132
allele frequency: 1.104620997840968e-3
allele num: 119498
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.300G>T
  hgvsp: ENST00000467425.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.300G>T
  hgvsp: ENST00000486284.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.300G>T
  hgvsp: ENST00000357716.4:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22532G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.300G>T
  hgvsp: ENST00000403881.1:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.300G>T
  hgvsp: ENST00000402647.2:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.300G>T
  hgvsp: ENST00000389335.3:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32984G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.300G>T
  hgvsp: ENST00000440923.3:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.300G>T
  hgvsp: ENST00000389336.4:c.300G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17377
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2192
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 27597
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr100Thr
num of homozygotes: 1
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ

3-6903381-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903381
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903381
    reference: chr 3
allele count: 1
allele frequency: 8.351149118118652e-6
allele num: 119744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22526C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.306C>T
  hgvsp: ENST00000440923.3:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.306C>T
  hgvsp: ENST00000357716.4:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.306C>T
  hgvsp: ENST00000402647.2:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.306C>T
  hgvsp: ENST00000389335.3:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32990C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.306C>T
  hgvsp: ENST00000389336.4:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.306C>T
  hgvsp: ENST00000486284.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.306C>T
  hgvsp: ENST00000403881.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.306C>T
  hgvsp: ENST00000467425.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27409
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17860
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly102Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

3-6903383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903383
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903383
    reference: chr 3
allele count: 1
allele frequency: 8.338753523123364e-6
allele num: 119922
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.308C>T
  hgvsp: ENSP00000385664.1:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.308C>T
  hgvsp: ENSP00000350348.4:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.308C>T
  hgvsp: ENSP00000373986.3:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.308C>T
  hgvsp: ENSP00000412329.3:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.308C>T
  hgvsp: ENSP00000373987.4:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32992C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.308C>T
  hgvsp: ENSP00000419835.1:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.308C>T
  hgvsp: ENSP00000384585.2:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.308C>T
  hgvsp: ENSP00000417536.1:p.Ala103Val
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22524C>T
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala103Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-6903384-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903384
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903384
    reference: chr 3
allele count: 3
allele frequency: 2.500208350695891e-5
allele num: 119990
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.309G>A
  hgvsp: ENST00000467425.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.309G>A
  hgvsp: ENST00000486284.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+32993G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.309G>A
  hgvsp: ENST00000357716.4:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.309G>A
  hgvsp: ENST00000440923.3:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22523G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.309G>A
  hgvsp: ENST00000402647.2:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.309G>A
  hgvsp: ENST00000403881.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.309G>A
  hgvsp: ENST00000389335.3:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.309G>A
  hgvsp: ENST00000389336.4:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7586
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27343
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8452
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala103Ala
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-6903394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903394
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903394
    reference: chr 3
allele count: 2
allele frequency: 1.65809981760902e-5
allele num: 120620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.319G>A
  hgvsp: ENSP00000412329.3:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.319G>A
  hgvsp: ENSP00000384585.2:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.319G>A
  hgvsp: ENSP00000419835.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22513G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.319G>A
  hgvsp: ENSP00000373987.4:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.319G>A
  hgvsp: ENSP00000417536.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.319G>A
  hgvsp: ENSP00000385664.1:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33003G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.319G>A
  hgvsp: ENSP00000373986.3:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.319G>A
  hgvsp: ENSP00000350348.4:p.Asp107Asn
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp107Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP

3-6903396-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903396
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903396
    reference: chr 3
allele count: 5
allele frequency: 4.142845306156268e-5
allele num: 120690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33005C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.321C>T
  hgvsp: ENST00000389336.4:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.321C>T
  hgvsp: ENST00000389335.3:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.321C>T
  hgvsp: ENST00000402647.2:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22511C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.321C>T
  hgvsp: ENST00000357716.4:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.321C>T
  hgvsp: ENST00000403881.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.321C>T
  hgvsp: ENST00000440923.3:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.321C>T
  hgvsp: ENST00000486284.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.321C>T
  hgvsp: ENST00000467425.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp107Asp
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD

3-6903397-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903397
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903397
    reference: chr 3
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.322A>T
  hgvsp: ENSP00000384585.2:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.322A>T
  hgvsp: ENSP00000350348.4:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.322A>T
  hgvsp: ENSP00000412329.3:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.322A>T
  hgvsp: ENSP00000373986.3:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.322A>T
  hgvsp: ENSP00000373987.4:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.322A>T
  hgvsp: ENSP00000419835.1:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.322A>T
  hgvsp: ENSP00000385664.1:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.322A>T
  hgvsp: ENSP00000417536.1:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33006A>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22510A>T
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr108Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-6903398-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903398
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903398
    reference: chr 3
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.323C>G
  hgvsp: ENSP00000373987.4:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.323C>G
  hgvsp: ENSP00000350348.4:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22509C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.323C>G
  hgvsp: ENSP00000373986.3:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.323C>G
  hgvsp: ENSP00000385664.1:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.323C>G
  hgvsp: ENSP00000417536.1:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.323C>G
  hgvsp: ENSP00000419835.1:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33007C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.323C>G
  hgvsp: ENSP00000384585.2:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.323C>G
  hgvsp: ENSP00000412329.3:p.Thr108Ser
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr108Ser
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

3-6903401-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903401
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903401
    reference: chr 3
allele count: 1
allele frequency: 8.276364358664525e-6
allele num: 120826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.326G>T
  hgvsp: ENSP00000419835.1:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33010G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.326G>T
  hgvsp: ENSP00000385664.1:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.326G>T
  hgvsp: ENSP00000384585.2:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.326G>T
  hgvsp: ENSP00000350348.4:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.326G>T
  hgvsp: ENSP00000417536.1:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.326G>T
  hgvsp: ENSP00000412329.3:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22506G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.326G>T
  hgvsp: ENSP00000373986.3:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.326G>T
  hgvsp: ENSP00000373987.4:p.Cys109Phe
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8120
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3793
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys109Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

3-6903402-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903402
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903402
    reference: chr 3
allele count: 1
allele frequency: 8.275679433281473e-6
allele num: 120836
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.327T>C
  hgvsp: ENST00000467425.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22505T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.327T>C
  hgvsp: ENST00000440923.3:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.327T>C
  hgvsp: ENST00000402647.2:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33011T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.327T>C
  hgvsp: ENST00000389335.3:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.327T>C
  hgvsp: ENST00000486284.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.327T>C
  hgvsp: ENST00000403881.1:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.327T>C
  hgvsp: ENST00000357716.4:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.327T>C
  hgvsp: ENST00000389336.4:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys109Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

3-6903424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903424
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903424
    reference: chr 3
allele count: 1
allele frequency: 8.255184255712587e-6
allele num: 121136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.349G>A
  hgvsp: ENSP00000417536.1:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33033G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.349G>A
  hgvsp: ENSP00000373987.4:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.349G>A
  hgvsp: ENSP00000385664.1:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.349G>A
  hgvsp: ENSP00000419835.1:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.349G>A
  hgvsp: ENSP00000350348.4:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.349G>A
  hgvsp: ENSP00000373986.3:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22483G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.349G>A
  hgvsp: ENSP00000384585.2:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.349G>A
  hgvsp: ENSP00000412329.3:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19356
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1131
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu117Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

3-6903436-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903436
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903436
    reference: chr 3
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.361A>G
  hgvsp: ENSP00000412329.3:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.361A>G
  hgvsp: ENSP00000419835.1:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.361A>G
  hgvsp: ENSP00000384585.2:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.361A>G
  hgvsp: ENSP00000385664.1:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33045A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.361A>G
  hgvsp: ENSP00000373987.4:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.361A>G
  hgvsp: ENSP00000417536.1:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.361A>G
  hgvsp: ENSP00000373986.3:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22471A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.361A>G
  hgvsp: ENSP00000350348.4:p.Thr121Ala
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr121Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

3-6903452-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903452
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903452
    reference: chr 3
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.377T>A
  hgvsp: ENSP00000350348.4:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22455T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.377T>A
  hgvsp: ENSP00000385664.1:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.377T>A
  hgvsp: ENSP00000373986.3:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.377T>A
  hgvsp: ENSP00000417536.1:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.377T>A
  hgvsp: ENSP00000384585.2:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.377T>A
  hgvsp: ENSP00000419835.1:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.377T>A
  hgvsp: ENSP00000412329.3:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33061T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.377T>A
  hgvsp: ENSP00000373987.4:p.Leu126His
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu126His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/3-6903464-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903464
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903464
    reference: chr 3
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.389A>C
  hgvsp: ENSP00000350348.4:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.389A>C
  hgvsp: ENSP00000373986.3:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.389A>C
  hgvsp: ENSP00000417536.1:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33073A>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.389A>C
  hgvsp: ENSP00000385664.1:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.389A>C
  hgvsp: ENSP00000373987.4:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.389A>C
  hgvsp: ENSP00000419835.1:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.389A>C
  hgvsp: ENSP00000384585.2:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.389A>C
  hgvsp: ENSP00000412329.3:p.Asp130Ala
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22443A>C
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp130Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum

3-6903468-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903468
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903468
    reference: chr 3
allele count: 2
allele frequency: 1.650246711883427e-5
allele num: 121194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.393C>T
  hgvsp: ENST00000402647.2:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.393C>T
  hgvsp: ENST00000486284.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.393C>T
  hgvsp: ENST00000467425.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33077C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.393C>T
  hgvsp: ENST00000389335.3:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.393C>T
  hgvsp: ENST00000403881.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.393C>T
  hgvsp: ENST00000440923.3:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.393C>T
  hgvsp: ENST00000389336.4:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.393C>T
  hgvsp: ENST00000357716.4:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22439C>T
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr131Thr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-6903474-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903474
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903474
    reference: chr 3
allele count: 2
allele frequency: 1.650328415354656e-5
allele num: 121188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.399C>A
  hgvsp: ENSP00000384585.2:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.399C>A
  hgvsp: ENSP00000419835.1:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.399C>A
  hgvsp: ENSP00000385664.1:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33083C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.399C>A
  hgvsp: ENSP00000417536.1:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.399C>A
  hgvsp: ENSP00000350348.4:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.399C>A
  hgvsp: ENSP00000373987.4:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.399C>A
  hgvsp: ENSP00000373986.3:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22433C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.399C>A
  hgvsp: ENSP00000412329.3:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27526
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3920
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp133Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

3-6903475-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903475
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903475
    reference: chr 3
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.400G>T
  hgvsp: ENSP00000373986.3:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.400G>T
  hgvsp: ENSP00000412329.3:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.400G>T
  hgvsp: ENSP00000417536.1:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.400G>T
  hgvsp: ENSP00000385664.1:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33084G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22432G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.400G>T
  hgvsp: ENSP00000373987.4:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.400G>T
  hgvsp: ENSP00000419835.1:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.400G>T
  hgvsp: ENSP00000384585.2:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.400G>T
  hgvsp: ENSP00000350348.4:p.Val134Leu
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val134Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

3-6903480-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903480
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903480
    reference: chr 3
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.405C>G
  hgvsp: ENST00000403881.1:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.405C>G
  hgvsp: ENST00000389335.3:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.405C>G
  hgvsp: ENST00000486284.1:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.405C>G
  hgvsp: ENST00000389336.4:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.405C>G
  hgvsp: ENST00000357716.4:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.405C>G
  hgvsp: ENST00000402647.2:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.405C>G
  hgvsp: ENST00000440923.3:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.405C>G
  hgvsp: ENST00000467425.1:c.405C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33089C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22427C>G
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg135Arg
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP

3-6903490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903490
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903490
    reference: chr 3
allele count: 1
allele frequency: 8.259684480052863e-6
allele num: 121070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.415G>A
  hgvsp: ENSP00000385664.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33099G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.415G>A
  hgvsp: ENSP00000350348.4:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.415G>A
  hgvsp: ENSP00000373987.4:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22417G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.415G>A
  hgvsp: ENSP00000412329.3:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.415G>A
  hgvsp: ENSP00000419835.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.415G>A
  hgvsp: ENSP00000373986.3:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.415G>A
  hgvsp: ENSP00000417536.1:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.415G>A
  hgvsp: ENSP00000384585.2:p.Gly139Ser
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly139Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

3-6903490-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903490
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903490
    reference: chr 3
allele count: 1
allele frequency: 8.259684480052863e-6
allele num: 121070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.415G>C
  hgvsp: ENSP00000419835.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.415G>C
  hgvsp: ENSP00000373986.3:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.415G>C
  hgvsp: ENSP00000417536.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.415G>C
  hgvsp: ENSP00000373987.4:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22417G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.415G>C
  hgvsp: ENSP00000384585.2:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33099G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.415G>C
  hgvsp: ENSP00000385664.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.415G>C
  hgvsp: ENSP00000412329.3:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.415G>C
  hgvsp: ENSP00000350348.4:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly139Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

3-6903493-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903493
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903493
    reference: chr 3
allele count: 6
allele frequency: 4.956711387218294e-5
allele num: 121048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33102G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.418G>C
  hgvsp: ENSP00000385664.1:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.418G>C
  hgvsp: ENSP00000373987.4:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.418G>C
  hgvsp: ENSP00000384585.2:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.418G>C
  hgvsp: ENSP00000412329.3:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.418G>C
  hgvsp: ENSP00000350348.4:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.418G>C
  hgvsp: ENSP00000417536.1:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.418G>C
  hgvsp: ENSP00000419835.1:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.418G>C
  hgvsp: ENSP00000373986.3:p.Glu140Gln
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22414G>C
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu140Gln
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

3-6903501-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903501
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903501
    reference: chr 3
allele count: 3
allele frequency: 2.479789713832267e-5
allele num: 120978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22406G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.426G>A
  hgvsp: ENST00000486284.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.426G>A
  hgvsp: ENST00000402647.2:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.426G>A
  hgvsp: ENST00000440923.3:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33110G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.426G>A
  hgvsp: ENST00000389336.4:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.426G>A
  hgvsp: ENST00000389335.3:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.426G>A
  hgvsp: ENST00000403881.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.426G>A
  hgvsp: ENST00000357716.4:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.426G>A
  hgvsp: ENST00000467425.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro142Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

3-6903501-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903501
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903501
    reference: chr 3
allele count: 2
allele frequency: 1.653193142554845e-5
allele num: 120978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.426G>T
  hgvsp: ENST00000403881.1:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22406G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.426G>T
  hgvsp: ENST00000440923.3:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.426G>T
  hgvsp: ENST00000402647.2:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.426G>T
  hgvsp: ENST00000357716.4:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.426G>T
  hgvsp: ENST00000467425.1:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.426G>T
  hgvsp: ENST00000389336.4:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.426G>T
  hgvsp: ENST00000486284.1:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33110G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.426G>T
  hgvsp: ENST00000389335.3:c.426G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8474
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro142Pro
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

3-6903514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903514
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903514
    reference: chr 3
allele count: 2
allele frequency: 1.656506758547575e-5
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.439C>T
  hgvsp: ENSP00000350348.4:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22393C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.439C>T
  hgvsp: ENSP00000373986.3:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.439C>T
  hgvsp: ENSP00000417536.1:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.439C>T
  hgvsp: ENSP00000419835.1:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.439C>T
  hgvsp: ENSP00000385664.1:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.439C>T
  hgvsp: ENSP00000412329.3:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33123C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.439C>T
  hgvsp: ENSP00000384585.2:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.439C>T
  hgvsp: ENSP00000373987.4:p.Pro147Ser
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro147Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

3-6903515-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903515
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903515
    reference: chr 3
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.440C>G
  hgvsp: ENSP00000384585.2:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.440C>G
  hgvsp: ENSP00000412329.3:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.440C>G
  hgvsp: ENSP00000417536.1:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.440C>G
  hgvsp: ENSP00000350348.4:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33124C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.440C>G
  hgvsp: ENSP00000419835.1:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.440C>G
  hgvsp: ENSP00000373986.3:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22392C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.440C>G
  hgvsp: ENSP00000385664.1:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.440C>G
  hgvsp: ENSP00000373987.4:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro147Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

3-6903516-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903516
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903516
    reference: chr 3
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.441G>A
  hgvsp: ENST00000403881.1:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.441G>A
  hgvsp: ENST00000467425.1:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.441G>A
  hgvsp: ENST00000389335.3:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.441G>A
  hgvsp: ENST00000486284.1:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.441G>A
  hgvsp: ENST00000389336.4:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33125G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22391G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.441G>A
  hgvsp: ENST00000440923.3:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.441G>A
  hgvsp: ENST00000357716.4:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.441G>A
  hgvsp: ENST00000402647.2:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27188
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4406
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro147Pro
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

3-6903519-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903519
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903519
    reference: chr 3
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.444G>T
  hgvsp: ENSP00000350348.4:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33128G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.444G>T
  hgvsp: ENSP00000385664.1:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.444G>T
  hgvsp: ENSP00000419835.1:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.444G>T
  hgvsp: ENSP00000417536.1:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.444G>T
  hgvsp: ENSP00000373987.4:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.444G>T
  hgvsp: ENSP00000384585.2:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22388G>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.444G>T
  hgvsp: ENSP00000412329.3:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.444G>T
  hgvsp: ENSP00000373986.3:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu148Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

3-6903526-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903526
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903526
    reference: chr 3
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.451G>C
  hgvsp: ENSP00000417536.1:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33135G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.451G>C
  hgvsp: ENSP00000419835.1:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.451G>C
  hgvsp: ENSP00000373986.3:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22381G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.451G>C
  hgvsp: ENSP00000412329.3:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.451G>C
  hgvsp: ENSP00000385664.1:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.451G>C
  hgvsp: ENSP00000373987.4:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.451G>C
  hgvsp: ENSP00000384585.2:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.451G>C
  hgvsp: ENSP00000350348.4:p.Val151Leu
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19316
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9041
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val151Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum

3-6903528-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903528
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903528
    reference: chr 3
allele count: 1
allele frequency: 8.304130474498016e-6
allele num: 120422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.453T>C
  hgvsp: ENST00000402647.2:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.453T>C
  hgvsp: ENST00000357716.4:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33137T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.453T>C
  hgvsp: ENST00000486284.1:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.453T>C
  hgvsp: ENST00000440923.3:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.453T>C
  hgvsp: ENST00000389335.3:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22379T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.453T>C
  hgvsp: ENST00000467425.1:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.453T>C
  hgvsp: ENST00000403881.1:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.453T>C
  hgvsp: ENST00000389336.4:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val151Val
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP

3-6903541-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903541
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903541
    reference: chr 3
allele count: 1
allele frequency: 8.323068215867098e-6
allele num: 120148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.466G>A
  hgvsp: ENSP00000373986.3:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.466G>A
  hgvsp: ENSP00000419835.1:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.466G>A
  hgvsp: ENSP00000373987.4:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.466G>A
  hgvsp: ENSP00000417536.1:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.466G>A
  hgvsp: ENSP00000350348.4:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22366G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.466G>A
  hgvsp: ENSP00000385664.1:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.466G>A
  hgvsp: ENSP00000384585.2:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.466G>A
  hgvsp: ENSP00000412329.3:p.Ala156Thr
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33150G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8423
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala156Thr
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

3-6903546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903546
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903546
    reference: chr 3
allele count: 1
allele frequency: 8.334722453742291e-6
allele num: 119980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.471G>A
  hgvsp: ENST00000440923.3:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.471G>A
  hgvsp: ENST00000486284.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.471G>A
  hgvsp: ENST00000357716.4:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.471G>A
  hgvsp: ENST00000389336.4:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33155G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.471G>A
  hgvsp: ENST00000389335.3:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.471G>A
  hgvsp: ENST00000467425.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.471G>A
  hgvsp: ENST00000403881.1:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22361G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.471G>A
  hgvsp: ENST00000402647.2:c.471G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser157Ser
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

3-6903549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903549
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903549
    reference: chr 3
allele count: 1
allele frequency: 8.340144451301897e-6
allele num: 119902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.474G>A
  hgvsp: ENST00000467425.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.474G>A
  hgvsp: ENST00000402647.2:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.474G>A
  hgvsp: ENST00000440923.3:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.474G>A
  hgvsp: ENST00000357716.4:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.474G>A
  hgvsp: ENST00000389335.3:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33158G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.474G>A
  hgvsp: ENST00000486284.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.474G>A
  hgvsp: ENST00000389336.4:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.474G>A
  hgvsp: ENST00000403881.1:c.474G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22358G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4384
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly158Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP

3-6903556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903556
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903556
    reference: chr 3
allele count: 1
allele frequency: 8.350591221858508e-6
allele num: 119752
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.481G>A
  hgvsp: ENSP00000419835.1:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22351G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.481G>A
  hgvsp: ENSP00000385664.1:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.481G>A
  hgvsp: ENSP00000373986.3:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33165G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.481G>A
  hgvsp: ENSP00000384585.2:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.481G>A
  hgvsp: ENSP00000412329.3:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.481G>A
  hgvsp: ENSP00000417536.1:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.481G>A
  hgvsp: ENSP00000373987.4:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.481G>A
  hgvsp: ENSP00000350348.4:p.Val161Ile
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val161Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-6903579-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903579
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903579
    reference: chr 3
allele count: 5
allele frequency: 4.196109367394552e-5
allele num: 119158
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.504C>A
  hgvsp: ENST00000440923.3:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.504C>A
  hgvsp: ENST00000402647.2:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.504C>A
  hgvsp: ENST00000467425.1:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22328C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.504C>A
  hgvsp: ENST00000357716.4:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.504C>A
  hgvsp: ENST00000486284.1:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33188C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.504C>A
  hgvsp: ENST00000403881.1:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.504C>A
  hgvsp: ENST00000389336.4:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.504C>A
  hgvsp: ENST00000389335.3:c.504C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile168Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

3-6903600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903600
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903600
    reference: chr 3
allele count: 1
allele frequency: 8.450513791238508e-6
allele num: 118336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33209G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+6G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22307G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16899
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 4.75e1
  variant carriers: 0
hgvs: c.519+6G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-6903600-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903600
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903599
    reference: chr 3
allele count: 3
allele frequency: 2.535154137371552e-5
allele num: 118336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33210delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22306delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+7delA
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25205
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.5e0
  variant carriers: 0
hgvs: c.519+7delA
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: GA
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-6903601-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903601
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903601
    reference: chr 3
allele count: 114715
allele frequency: 9.683042120368026e-1
allele num: 118470
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33210A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22306A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+7A>G
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 9.75e1
  variant carriers: 1684
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 2.75e1
  variant carriers: 2709
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 7.5e0
  variant carriers: 1151
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 5.25e1
  variant carriers: 6840
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 1.25e1
  variant carriers: 2145
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 7.25e1
  variant carriers: 1982
genotype depth: GenotypeDepth
  all individuals: 3977
  bin: 3.25e1
  variant carriers: 3972
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 5.75e1
  variant carriers: 5513
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 6.25e1
  variant carriers: 4077
genotype depth: GenotypeDepth
  all individuals: 5512
  bin: 3.75e1
  variant carriers: 5511
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 6.75e1
  variant carriers: 2880
genotype depth: GenotypeDepth
  all individuals: 6837
  bin: 4.25e1
  variant carriers: 6837
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.25e1
  variant carriers: 2068
genotype depth: GenotypeDepth
  all individuals: 2321
  bin: 1.75e1
  variant carriers: 2320
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 4.75e1
  variant carriers: 7311
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.75e1
  variant carriers: 650
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 478
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 8.25e1
  variant carriers: 877
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 7.75e1
  variant carriers: 1310
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
hgvs: c.519+7A>G
num of homozygotes: 55574
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP

3-6903604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903604
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903604
    reference: chr 3
allele count: 1
allele frequency: 8.832673827020915e-6
allele num: 113216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22303C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33213C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+10C>T
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

3-6903605-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903605
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903605
    reference: chr 3
allele count: 1
allele frequency: 8.851750876323337e-6
allele num: 112972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33214G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22302G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+11G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13499
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

3-6903620-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903620
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903620
    reference: chr 3
allele count: 1
allele frequency: 9.103488456776638e-6
allele num: 109848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22287G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33229G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+26G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6604
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6777
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22316
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2576
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-6903626-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903626
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903626
    reference: chr 3
allele count: 3
allele frequency: 2.763296059539819e-5
allele num: 108566
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33235A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22281A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+32A>G
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18515
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-6903632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903632
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903632
    reference: chr 3
allele count: 1
allele frequency: 9.325922333718804e-6
allele num: 107228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22275G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33241G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+38G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 4.25e1
  variant carriers: 0
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: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff

3-6903645-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6903645
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6903645
    reference: chr 3
allele count: 1
allele frequency: 9.609655782129884e-6
allele num: 104062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-22262T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+33254T>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+51T>C
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12916
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3225
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2049
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4912
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-6904640-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6904640
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6904640
    reference: chr 3
allele count: 1
allele frequency: 8.21827744904668e-5
allele num: 12168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000405194
  ensembl transcript: ENST00000435689
  gene symbol: GRM7
  hgvsc: ENST00000435689.1:c.-28C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+34249C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-21267C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+1046C>G
  variant of: http://identifiers.org/hgnc/4599
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/3-6904664-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6904664
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6904664
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 12260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+34273C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000405194
  ensembl transcript: ENST00000435689
  gene symbol: GRM7
  hgvsc: ENST00000435689.1:c.-4C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-21243C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+1070C>A
  variant of: http://identifiers.org/hgnc/4599
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13240
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum

3-6904665-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6904665
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6904665
    reference: chr 3
allele count: 1
allele frequency: 8.152616990053807e-5
allele num: 12266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+34274C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000405194
  ensembl transcript: ENST00000435689
  gene symbol: GRM7
  hgvsc: ENST00000435689.1:c.-3C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-21242C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+1071C>G
  variant of: http://identifiers.org/hgnc/4599
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum

3-6904697-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6904697
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6904697
    reference: chr 3
allele count: 1
allele frequency: 8.164598301763554e-5
allele num: 12248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+34306G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000405194
  ensembl transcript: ENST00000435689
  gene symbol: GRM7
  hgvsc: ENST00000435689.1:c.21+9G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-21210G>C
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+1103G>C
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

3-6904719-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6904719
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6904719
    reference: chr 3
allele count: 4
allele frequency: 3.274394237066143e-4
allele num: 12216
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000405194
  ensembl transcript: ENST00000435689
  gene symbol: GRM7
  hgvsc: ENST00000435689.1:c.21+31T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-21188T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+34328T>G
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+1125T>G
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

3-6904731-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6904731
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6904731
    reference: chr 3
allele count: 4
allele frequency: 3.278688524590164e-4
allele num: 12200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+34340G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000405194
  ensembl transcript: ENST00000435689
  gene symbol: GRM7
  hgvsc: ENST00000435689.1:c.21+43G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+1137G>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*29-21176G>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

3-6998224-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 6998224
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 6998224
    reference: chr 3
allele count: 1
allele frequency: 8.144648965629581e-5
allele num: 12278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000412329
  ensembl transcript: ENST00000440923
  gene symbol: GRM7
  hgvsc: ENST00000440923.3:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000417536
  ensembl transcript: ENST00000486284
  gene symbol: GRM7
  hgvsc: ENST00000486284.1:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000405194
  ensembl transcript: ENST00000435689
  gene symbol: GRM7
  hgvsc: ENST00000435689.1:c.22-30T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000419835
  ensembl transcript: ENST00000467425
  gene symbol: GRM7
  hgvsc: ENST00000467425.1:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373987
  ensembl transcript: ENST00000389336
  gene symbol: GRM7
  hgvsc: ENST00000389336.4:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000385664
  ensembl transcript: ENST00000403881
  gene symbol: GRM7
  hgvsc: ENST00000403881.1:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000393799
  ensembl transcript: ENST00000448328
  gene symbol: GRM7
  hgvsc: ENST00000448328.2:c.-106+127833T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000384585
  ensembl transcript: ENST00000402647
  gene symbol: GRM7
  hgvsc: ENST00000402647.2:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000373986
  ensembl transcript: ENST00000389335
  gene symbol: GRM7
  hgvsc: ENST00000389335.3:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000404161
  ensembl transcript: ENST00000443259
  gene symbol: GRM7
  hgvsc: ENST00000443259.1:c.*115+72231T>A
  variant of: http://identifiers.org/hgnc/4599
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000196277
  ensembl protein: ENSP00000350348
  ensembl transcript: ENST00000357716
  gene symbol: GRM7
  hgvsc: ENST00000357716.4:c.519+94630T>A
  variant of: http://identifiers.org/hgnc/4599
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14932
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2394
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1689
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2508
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1043
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 438
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28410
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3496
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6924
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.896381703709323e-5
allele num: 52732
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 5.611e0

VQSLOD
type: SiteQuality
SIO_000300: -4.52e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

DP
type: SiteQuality
SIO_000300: 1.08939e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

QD
type: SiteQuality
SIO_000300: 4.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

GenotypeQuality
all individuals: 1388
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 13584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3801
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2321
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29112
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 1.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.850686604730355e-5
allele num: 54034
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9140
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8002
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7074
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.848e1

FS
type: SiteQuality
SIO_000300: 6.561e0

VQSLOD
type: SiteQuality
SIO_000300: -1.961e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

DP
type: SiteQuality
SIO_000300: 1.117747e6

GenotypeQuality
all individuals: 269
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.25e1
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GenotypeQuality
all individuals: 1308
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29079
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7104
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.241002730206007e-4
allele num: 8058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4696
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.412e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.432e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 1.127612e6

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.69e-1

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 2.02e-1

GenotypeQuality
all individuals: 303
bin: 1.75e1
variant carriers: 186

GenotypeQuality
all individuals: 1075
bin: 3.75e1
variant carriers: 570

GenotypeQuality
all individuals: 12872
bin: 6.25e1
variant carriers: 912

GenotypeQuality
all individuals: 1225
bin: 7.75e1
variant carriers: 792

GenotypeQuality
all individuals: 957
bin: 8.25e1
variant carriers: 750

GenotypeQuality
all individuals: 1216
bin: 4.75e1
variant carriers: 848

GenotypeQuality
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bin: 7.5e0
variant carriers: 126

GenotypeQuality
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bin: 3.25e1
variant carriers: 473

GenotypeQuality
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bin: 4.25e1
variant carriers: 426

GenotypeQuality
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bin: 1.25e1
variant carriers: 156

GenotypeQuality
all individuals: 501
bin: 8.75e1
variant carriers: 449

GenotypeQuality
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bin: 2.75e1
variant carriers: 247

GenotypeQuality
all individuals: 652
bin: 9.25e1
variant carriers: 603

GenotypeQuality
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variant carriers: 253

GenotypeQuality
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variant carriers: 28779

GenotypeQuality
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bin: 5.75e1
variant carriers: 578

GenotypeQuality
all individuals: 2357
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variant carriers: 856

GenotypeQuality
all individuals: 1452
bin: 5.25e1
variant carriers: 926

GenotypeQuality
all individuals: 960
bin: 7.25e1
variant carriers: 500

Latino
type: Population
allele count: 4503
allele frequency: 4.209985041136873e-1
allele num: 10696
num of homozygotes: 835

European (Finnish)
type: Population
allele count: 2300
allele frequency: 3.977862331373228e-1
allele num: 5782
num of homozygotes: 412

African
type: Population
allele count: 3277
allele frequency: 3.518359458879107e-1
allele num: 9314
num of homozygotes: 537

Other
type: Population
allele count: 370
allele frequency: 4.457831325301205e-1
allele num: 830
num of homozygotes: 87

European (Non-Finnish)
type: Population
allele count: 24920
allele frequency: 4.048346221326922e-1
allele num: 61556
num of homozygotes: 4788

East Asian
type: Population
allele count: 2424
allele frequency: 3.042932462967612e-1
allele num: 7966
num of homozygotes: 328

South Asian
type: Population
allele count: 9031
allele frequency: 5.669889502762431e-1
allele num: 15928
num of homozygotes: 2557

FS
type: SiteQuality
SIO_000300: 5.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.78e-2

DP
type: SiteQuality
SIO_000300: 1.483203e6

QD
type: SiteQuality
SIO_000300: 1.713e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.89e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1895
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2731
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1545
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variant carriers: 0

GenotypeQuality
all individuals: 5865
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variant carriers: 0

GenotypeQuality
all individuals: 50
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2112
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variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 2375
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variant carriers: 0

GenotypeQuality
all individuals: 2745
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variant carriers: 19

GenotypeQuality
all individuals: 2279
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variant carriers: 1

GenotypeQuality
all individuals: 2686
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2849
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variant carriers: 0

GenotypeQuality
all individuals: 24295
bin: 6.25e1
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GenotypeQuality
all individuals: 5023
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variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62596
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.768633345859953e-4
allele num: 15966
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.625815808556925e-4
allele num: 11032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6000
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.182033096926714e-3
allele num: 846
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

FS
type: SiteQuality
SIO_000300: 5.473e0

QD
type: SiteQuality
SIO_000300: 1.496e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.747e0

DP
type: SiteQuality
SIO_000300: 1.393327e6

GenotypeQuality
all individuals: 2941
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24700
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
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variant carriers: 0

GenotypeQuality
all individuals: 1985
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variant carriers: 0

GenotypeQuality
all individuals: 2363
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 2697
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variant carriers: 0

GenotypeQuality
all individuals: 2724
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variant carriers: 1

GenotypeQuality
all individuals: 246
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variant carriers: 0

GenotypeQuality
all individuals: 751
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variant carriers: 0

GenotypeQuality
all individuals: 569
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GenotypeQuality
all individuals: 188
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GenotypeQuality
all individuals: 4822
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GenotypeQuality
all individuals: 131
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variant carriers: 0

GenotypeQuality
all individuals: 2778
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variant carriers: 0

GenotypeQuality
all individuals: 1562
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variant carriers: 0

GenotypeQuality
all individuals: 2256
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variant carriers: 0

GenotypeQuality
all individuals: 5782
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5939303133667e-5
allele num: 62738
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.021e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.273e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.398837e6

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

GenotypeQuality
all individuals: 271
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
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variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
all individuals: 2290
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variant carriers: 0

GenotypeQuality
all individuals: 2539
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 1563
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variant carriers: 0

GenotypeQuality
all individuals: 5815
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variant carriers: 0

GenotypeQuality
all individuals: 1564
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variant carriers: 0

GenotypeQuality
all individuals: 4686
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
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variant carriers: 0

GenotypeQuality
all individuals: 1882
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variant carriers: 0

GenotypeQuality
all individuals: 33
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GenotypeQuality
all individuals: 708
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variant carriers: 0

GenotypeQuality
all individuals: 2723
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 979
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11082
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.243756243756244e-5
allele num: 16016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9532
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.34e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

DP
type: SiteQuality
SIO_000300: 1.403184e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.99e-1

QD
type: SiteQuality
SIO_000300: 1.63e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1569
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variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590027348470394e-5
allele num: 62892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11086
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

QD
type: SiteQuality
SIO_000300: 6.74e0

DP
type: SiteQuality
SIO_000300: 1.405308e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.678e0

VQSLOD
type: SiteQuality
SIO_000300: -7.047e-1

FS
type: SiteQuality
SIO_000300: 2.675e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

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

GenotypeQuality
all individuals: 405
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GenotypeQuality
all individuals: 79
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2455
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variant carriers: 0

GenotypeQuality
all individuals: 6040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.176470588235294e-3
allele num: 850
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.416594e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.2755e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.712e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

QD
type: SiteQuality
SIO_000300: 9.19e0

MQRankSum
type: SiteQuality
SIO_000300: 5.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.08e-1

GenotypeQuality
all individuals: 1366
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 28018
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GenotypeQuality
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GenotypeQuality
all individuals: 735
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GenotypeQuality
all individuals: 3891
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GenotypeQuality
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GenotypeQuality
all individuals: 124
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GenotypeQuality
all individuals: 961
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GenotypeQuality
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GenotypeQuality
all individuals: 780
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
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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bin: 8.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16114
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.569168968114487e-5
allele num: 63728
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11186
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6160
num of homozygotes: 0

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

DP
type: SiteQuality
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VQSLOD
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MQRankSum
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SIO_000300: 2.69e-1

BaseQRankSum
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SIO_000300: -2.327e0

QD
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FS
type: SiteQuality
SIO_000300: 2.142e0

InbreedingCoeff
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2615
bin: 7.25e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.235330450895614e-4
allele num: 16190
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560987793075458e-5
allele num: 64062
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11234
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 1.461643e6

VQSLOD
type: SiteQuality
SIO_000300: 2.21e-1

MQRankSum
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SIO_000300: 2.29e-1

FS
type: SiteQuality
SIO_000300: 2.111e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 1.82e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 1.013581998783702e-4
allele num: 9866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64188
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -7.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.339e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

DP
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SIO_000300: 1.46966e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.77e-1

QD
type: SiteQuality
SIO_000300: 5.98e0

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

GenotypeQuality
all individuals: 811
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.155361319709468e-5
allele num: 16246
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11266
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: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQ
type: SiteQuality
SIO_000300: 5.801e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.49e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 1.477635e6

QD
type: SiteQuality
SIO_000300: 1.181e1

VQSLOD
type: SiteQuality
SIO_000300: -1.664e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 9
allele frequency: 1.424501424501425e-3
allele num: 6318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548083472660846e-5
allele num: 64596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.575e0

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.681e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.223e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64614
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 6.144015728680265e-5
allele num: 16276
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

MQRankSum
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DP
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -7.0e-4

MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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QD
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SIO_000300: 1.241e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.691361063253754e-5
allele num: 65008
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6384
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African
type: Population
allele count: 0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.519741e6

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 1
allele frequency: 9.948269001193792e-5
allele num: 10052
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65126
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

QD
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SIO_000300: 9.08e0

VQSLOD
type: SiteQuality
SIO_000300: 1.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.52e-1

DP
type: SiteQuality
SIO_000300: 1.526168e6

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3280
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variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65472
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.753501400560224e-5
allele num: 11424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.89e0

VQSLOD
type: SiteQuality
SIO_000300: -1.378e0

BaseQRankSum
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SIO_000300: 4.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

DP
type: SiteQuality
SIO_000300: 1.54758e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.859988168014199e-5
allele num: 10142
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65594
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

QD
type: SiteQuality
SIO_000300: 1.028e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 6.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.554406e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 131

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3341
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168224299065421e-4
allele num: 8560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65612
num of homozygotes: 0

South Asian
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allele count: 131
allele frequency: 7.998534619611674e-3
allele num: 16378
num of homozygotes: 1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 5.610000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.28e0

QD
type: SiteQuality
SIO_000300: 1.335e1

DP
type: SiteQuality
SIO_000300: 1.561375e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 8235
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52077376969402e-5
allele num: 65756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
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VQSLOD
type: SiteQuality
SIO_000300: 5.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

DP
type: SiteQuality
SIO_000300: 1.569211e6

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-1

FS
type: SiteQuality
SIO_000300: 1.762e0

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

QD
type: SiteQuality
SIO_000300: 1.026e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8422
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.0960741282614e-5
allele num: 16404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65844
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.522e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 7.2e-3

BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
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SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.574705e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.91e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.73e-1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65896
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.828153564899452e-4
allele num: 16410
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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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GenotypeQuality
all individuals: 2930
bin: 9.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017774692941425e-5
allele num: 66274
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.51e-1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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QD
type: SiteQuality
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

Latino
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allele count: 5
allele frequency: 4.341031429067547e-4
allele num: 11518
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

VQSLOD
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SIO_000300: 6.61e-1

ClippingRankSum
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SIO_000300: 1.38e-1

MQRankSum
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SIO_000300: 4.34e-1

InbreedingCoeff
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SIO_000300: 4.59e-2

BaseQRankSum
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SIO_000300: -4.098e0

ReadPosRankSum
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.99e-1

DP
type: SiteQuality
SIO_000300: 1.603004e6

QD
type: SiteQuality
SIO_000300: 1.553e1

GenotypeQuality
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bin: 7.75e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66350
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.801e0

QD
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MQ
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ClippingRankSum
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SIO_000300: 6.919999999999999e-1

MQRankSum
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SIO_000300: 1.92e0

FS
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SIO_000300: 3.152e0

BaseQRankSum
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SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 1.603996e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10328
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 1.34e-2

QD
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SIO_000300: 9.970000000000001e0

MQRankSum
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FS
type: SiteQuality
SIO_000300: 2.1179e1

MQ
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SIO_000300: 5.858e1

VQSLOD
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SIO_000300: -3.061e0

ClippingRankSum
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SIO_000300: -7.9e-2

BaseQRankSum
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SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.41e-1

DP
type: SiteQuality
SIO_000300: 1.604959e6

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50652324565368e-5
allele num: 66378
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: 10340
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.572e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

FS
type: SiteQuality
SIO_000300: 9.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.607206e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.619999999999999e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66384
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

BaseQRankSum
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SIO_000300: 2.51e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.607806e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6608
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 10376
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.98e-1

FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.378e-1

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

QD
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ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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South Asian
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allele frequency: 6.05766900896535e-5
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e0

FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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MQ
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
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Other
type: Population
allele count: 0
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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FS
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MQRankSum
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QD
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

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

African
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allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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BaseQRankSum
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SIO_000300: 3.45e0

ClippingRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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VQSLOD
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SIO_000300: 5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
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FS
type: SiteQuality
SIO_000300: 2.069e0

ReadPosRankSum
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SIO_000300: 1.65e0

MQRankSum
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SIO_000300: 1.0e0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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QD
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VQSLOD
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SIO_000300: 4.18e-1

MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -8.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.05766900896535e-5
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num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
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MQ
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SIO_000300: 5.988e1

VQSLOD
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ClippingRankSum
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SIO_000300: -1.99e-1

FS
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DP
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MQRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.343e0

MQRankSum
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SIO_000300: 4.78e-1

BaseQRankSum
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SIO_000300: 2.53e0

ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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SIO_000300: 1.031e1

DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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FS
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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DP
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SIO_000300: 1.621751e6

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502945773716484e-5
allele num: 66536
num of homozygotes: 0

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

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 904
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East Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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InbreedingCoeff
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QD
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VQSLOD
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MQRankSum
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FS
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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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

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

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

South Asian
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allele count: 0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

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

Other
type: Population
allele count: 1
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allele num: 904
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.51653638003608e-5
allele num: 66520
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10304
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European (Finnish)
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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

MQRankSum
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SIO_000300: -6.8e-2

QD
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SIO_000300: 1.249e1

ReadPosRankSum
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SIO_000300: 4.79e-1

DP
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SIO_000300: 1.620916e6

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.51304269338388e-5
allele num: 66474
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 1.64e-1

InbreedingCoeff
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SIO_000300: 3.0e-4

VQSLOD
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FS
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SIO_000300: 1.725e0

MQ
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SIO_000300: 5.971e1

QD
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DP
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SIO_000300: 1.620311e6

MQRankSum
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SIO_000300: -1.82e-1

BaseQRankSum
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SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.941370607649e-4
allele num: 10302
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66474
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.64e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
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SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

FS
type: SiteQuality
SIO_000300: 1.725e0

DP
type: SiteQuality
SIO_000300: 1.620311e6

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.316423442205235e-4
allele num: 8634
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.58e0

VQSLOD
type: SiteQuality
SIO_000300: -3.4e-3

FS
type: SiteQuality
SIO_000300: 4.277e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 9.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.727e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

DP
type: SiteQuality
SIO_000300: 1.617422e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 906
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10250
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.507840772014475e-5
allele num: 66320
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.617158e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508477644361311e-5
allele num: 66292
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

South Asian
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East Asian
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allele num: 8630
num of homozygotes: 0

Other
type: Population
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Latino
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allele count: 0
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African
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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QD
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FS
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MQRankSum
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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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GenotypeQuality
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variant carriers: 0

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

Other
type: Population
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num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

East Asian
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African
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South Asian
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QD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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DP
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BaseQRankSum
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.511213201958532e-5
allele num: 66172
num of homozygotes: 0

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

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

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

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

ClippingRankSum
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SIO_000300: 1.57e-1

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: 2.78e-1

QD
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VQSLOD
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MQ
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SIO_000300: 5.918e1

MQRankSum
type: SiteQuality
SIO_000300: 1.56e0

FS
type: SiteQuality
SIO_000300: 2.796e0

DP
type: SiteQuality
SIO_000300: 1.613758e6

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.130456105934282e-5
allele num: 16312
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
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SIO_000300: -4.4e-2

FS
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SIO_000300: 2.318e0

QD
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InbreedingCoeff
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SIO_000300: 2.0e-4

ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

VQSLOD
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BaseQRankSum
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SIO_000300: -8.03e-1

DP
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SIO_000300: 1.60795e6

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515151515151515e-5
allele num: 66000
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10108
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South Asian
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allele frequency: 0.0e0
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 6.6e-3

DP
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ClippingRankSum
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SIO_000300: 1.05e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.165228113440197e-5
allele num: 16220
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65974
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -3.447e0

QD
type: SiteQuality
SIO_000300: 1.481e1

MQRankSum
type: SiteQuality
SIO_000300: -6.29e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.11e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.601653e6

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 1
allele frequency: 9.956192751891676e-5
allele num: 10044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65934
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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MQ
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FS
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QD
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6610
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65754
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 4.351610095735422e-4
allele num: 11490
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VQSLOD
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DP
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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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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num of homozygotes: 0

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

East Asian
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South Asian
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Latino
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allele frequency: 8.709284096847239e-5
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num of homozygotes: 0

European (Non-Finnish)
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Other
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QD
type: SiteQuality
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
type: Population
allele count: 0
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allele num: 65524
num of homozygotes: 0

African
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allele count: 0
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South Asian
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allele frequency: 1.944516463572725e-4
allele num: 15428
num of homozygotes: 0

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

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

FS
type: SiteQuality
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QD
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 1.553707e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.06e-1

GenotypeQuality
all individuals: 878
bin: 5.25e1
variant carriers: 877

GenotypeQuality
all individuals: 862
bin: 6.25e1
variant carriers: 793

GenotypeQuality
all individuals: 336
bin: 2.75e1
variant carriers: 336

GenotypeQuality
all individuals: 48733
bin: 9.75e1
variant carriers: 48733

GenotypeQuality
all individuals: 915
bin: 3.75e1
variant carriers: 914

GenotypeQuality
all individuals: 123
bin: 1.25e1
variant carriers: 123

GenotypeQuality
all individuals: 1354
bin: 9.25e1
variant carriers: 1354

GenotypeQuality
all individuals: 338
bin: 1.75e1
variant carriers: 338

GenotypeQuality
all individuals: 472
bin: 2.25e1
variant carriers: 463

GenotypeQuality
all individuals: 934
bin: 4.75e1
variant carriers: 934

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 99

GenotypeQuality
all individuals: 446
bin: 5.75e1
variant carriers: 445

GenotypeQuality
all individuals: 933
bin: 7.75e1
variant carriers: 931

GenotypeQuality
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bin: 4.25e1
variant carriers: 466

GenotypeQuality
all individuals: 680
bin: 8.75e1
variant carriers: 680

GenotypeQuality
all individuals: 797
bin: 6.75e1
variant carriers: 787

GenotypeQuality
all individuals: 1073
bin: 8.25e1
variant carriers: 1073

GenotypeQuality
all individuals: 719
bin: 3.25e1
variant carriers: 717

GenotypeQuality
all individuals: 457
bin: 7.25e1
variant carriers: 454

African
type: Population
allele count: 9775
allele frequency: 9.931924405608616e-1
allele num: 9842
num of homozygotes: 4854

European (Finnish)
type: Population
allele count: 6309
allele frequency: 9.550408719346049e-1
allele num: 6606
num of homozygotes: 3010

South Asian
type: Population
allele count: 15356
allele frequency: 9.91349257585539e-1
allele num: 15490
num of homozygotes: 7612

Other
type: Population
allele count: 849
allele frequency: 9.691780821917808e-1
allele num: 876
num of homozygotes: 411

Latino
type: Population
allele count: 11311
allele frequency: 9.851071241943912e-1
allele num: 11482
num of homozygotes: 5571

East Asian
type: Population
allele count: 8600
allele frequency: 1.0e0
allele num: 8600
num of homozygotes: 4300

European (Non-Finnish)
type: Population
allele count: 62515
allele frequency: 9.533504132735535e-1
allele num: 65574
num of homozygotes: 29816

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.77e-2

FS
type: SiteQuality
SIO_000300: 8.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

QD
type: SiteQuality
SIO_000300: 3.31e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.885666e6

GenotypeQuality
all individuals: 32307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1005
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 203
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.178411501296253e-4
allele num: 8486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

DP
type: SiteQuality
SIO_000300: 1.643195e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: 7.21e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 9.76e0

GenotypeQuality
all individuals: 385
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 812
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variant carriers: 0

GenotypeQuality
all individuals: 8200
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 764
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variant carriers: 0

GenotypeQuality
all individuals: 179
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 130
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2431
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variant carriers: 0

GenotypeQuality
all individuals: 120
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variant carriers: 0

GenotypeQuality
all individuals: 817
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variant carriers: 0

GenotypeQuality
all individuals: 1732
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variant carriers: 0

GenotypeQuality
all individuals: 2775
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variant carriers: 0

GenotypeQuality
all individuals: 5192
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63898
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.065416577881952e-4
allele num: 9386
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.448e0

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

DP
type: SiteQuality
SIO_000300: 1.636845e6

MQRankSum
type: SiteQuality
SIO_000300: 5.82e-1

QD
type: SiteQuality
SIO_000300: 1.51e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.67e-1

GenotypeQuality
all individuals: 306
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
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variant carriers: 0

GenotypeQuality
all individuals: 7085
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variant carriers: 0

GenotypeQuality
all individuals: 787
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variant carriers: 0

GenotypeQuality
all individuals: 27906
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variant carriers: 0

GenotypeQuality
all individuals: 295
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variant carriers: 0

GenotypeQuality
all individuals: 2054
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variant carriers: 0

GenotypeQuality
all individuals: 6787
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variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2125
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variant carriers: 0

GenotypeQuality
all individuals: 405
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variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 630
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variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
all individuals: 2493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11174
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11166
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.594336915276936e-5
allele num: 62722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.723e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.037e-1

DP
type: SiteQuality
SIO_000300: 1.524862e6

MQRankSum
type: SiteQuality
SIO_000300: -1.747e0

QD
type: SiteQuality
SIO_000300: 1.223e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

GenotypeQuality
all individuals: 22491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
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variant carriers: 0

GenotypeQuality
all individuals: 777
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 161
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GenotypeQuality
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GenotypeQuality
all individuals: 2571
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2343
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 641
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variant carriers: 0

GenotypeQuality
all individuals: 967
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GenotypeQuality
all individuals: 3676
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variant carriers: 0

GenotypeQuality
all individuals: 1927
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GenotypeQuality
all individuals: 5895
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GenotypeQuality
all individuals: 1545
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variant carriers: 0

GenotypeQuality
all individuals: 889
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.820361205733016e-5
allele num: 62236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10606
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.935e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.437535e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.32e0

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

GenotypeQuality
all individuals: 4626
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variant carriers: 0

GenotypeQuality
all individuals: 4693
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GenotypeQuality
all individuals: 902
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4818
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.8405825624877e-5
allele num: 10162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8992
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.360624e6

VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.739e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
SIO_000300: 1.229e1

FS
type: SiteQuality
SIO_000300: 1.013e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

GenotypeQuality
all individuals: 4901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2872
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variant carriers: 0

GenotypeQuality
all individuals: 535
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 767
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GenotypeQuality
all individuals: 1457
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GenotypeQuality
all individuals: 2556
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.07e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

QD
type: SiteQuality
SIO_000300: 1.455e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

DP
type: SiteQuality
SIO_000300: 1.28754e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.8e-1

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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variant carriers: 0

GenotypeQuality
all individuals: 567
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 125
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GenotypeQuality
all individuals: 215
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variant carriers: 0

GenotypeQuality
all individuals: 69
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3028
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GenotypeQuality
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GenotypeQuality
all individuals: 362
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GenotypeQuality
all individuals: 2701
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GenotypeQuality
all individuals: 218
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GenotypeQuality
all individuals: 71
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.332977872567315e-4
allele num: 7502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

InbreedingCoeff
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FS
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
SIO_000300: 1.968e1

MQ
type: SiteQuality
SIO_000300: 5.804e1

DP
type: SiteQuality
SIO_000300: 2.33249e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

VQSLOD
type: SiteQuality
SIO_000300: -5.221e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Finnish)
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DP
type: SiteQuality
SIO_000300: 2.31222e5

VQSLOD
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BaseQRankSum
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SIO_000300: -7.31e-1

MQRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.75e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

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

European (Finnish)
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VQSLOD
type: SiteQuality
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DP
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SIO_000300: 2.31319e5

BaseQRankSum
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SIO_000300: -8.05e-1

InbreedingCoeff
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SIO_000300: -7.74e-2

ReadPosRankSum
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MQRankSum
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FS
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QD
type: SiteQuality
SIO_000300: 7.05e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-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
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3572
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 562
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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num of homozygotes: 0

South Asian
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allele num: 7580
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -1.722e0

VQSLOD
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MQ
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FS
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 2.66e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3556
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 5.285412262156448e-4
allele num: 7568
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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Other
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BaseQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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QD
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