14-72961999-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72961999
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72961999
    reference: chr 14
allele count: 72
allele frequency: 5.938732080700771e-4
allele num: 121238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-14863G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.758+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.548+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.965+29G>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7237
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8632
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7452
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

14-72962008-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72962008
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72962008
    reference: chr 14
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.758+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-14854T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.548+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.965+38T>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

14-72962008-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72962008
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72962008
    reference: chr 14
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.758+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.548+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-14854T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.965+38T>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

14-72962009-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72962009
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72962009
    reference: chr 14
allele count: 3
allele frequency: 2.477250582153887e-5
allele num: 121102
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-14853A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.548+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.758+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.965+39A>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/14-72962014-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72962014
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72962014
    reference: chr 14
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.548+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.758+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-14848A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.965+44A>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6619
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

14-72962018-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72962018
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72962018
    reference: chr 14
allele count: 1
allele frequency: 8.265145879824779e-6
allele num: 120990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.758+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-14844T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.548+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.965+48T>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7217
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS

14-72962021-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72962021
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72962021
    reference: chr 14
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.758+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-14841A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.548+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.965+51A>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

14-72976811-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976811
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976811
    reference: chr 14
allele count: 1
allele frequency: 9.01859634566476e-6
allele num: 110882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-51A>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2036
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS

14-72976818-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976818
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976818
    reference: chr 14
allele count: 1
allele frequency: 9.01599437401951e-6
allele num: 110914
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-44C>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-44C>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-72976823-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976823
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976823
    reference: chr 14
allele count: 1
allele frequency: 9.012419113538457e-6
allele num: 110958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-39G>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-39G>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

14-72976825-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976825
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976825
    reference: chr 14
allele count: 1
allele frequency: 9.005277092376133e-6
allele num: 111046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-37A>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

14-72976826-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976826
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976826
    reference: chr 14
allele count: 1
allele frequency: 9.003331232556045e-6
allele num: 111070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-36T>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7863
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

14-72976835-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976835
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976835
    reference: chr 14
allele count: 2
allele frequency: 1.794977652528226e-5
allele num: 111422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-27T>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2260
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

14-72976847-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976847
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976847
    reference: chr 14
allele count: 18
allele frequency: 1.602278796510593e-4
allele num: 112340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-15T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-15T>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7865
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

14-72976849-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976849
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976849
    reference: chr 14
allele count: 1
allele frequency: 8.879890599747811e-6
allele num: 112614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-13C>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

14-72976850-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976850
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976850
    reference: chr 14
allele count: 1
allele frequency: 8.862733976176972e-6
allele num: 112832
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-12T>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-72976852-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976852
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976852
    reference: chr 14
allele count: 27
allele frequency: 2.388873159682899e-4
allele num: 113024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-10C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-10C>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7854
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/14-72976858-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976858
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976858
    reference: chr 14
allele count: 1
allele frequency: 8.7363712608331e-6
allele num: 114464
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.759-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.855-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.966-4A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.549-4A>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.966-4A>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

14-72976866-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976866
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976866
    reference: chr 14
allele count: 1
allele frequency: 8.636175210722675e-6
allele num: 115792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.970G>A
  hgvsp: ENSP00000384612.4:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.970G>A
  hgvsp: ENSP00000451030.1:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.859G>A
  hgvsp: ENSP00000341199.6:p.Glu287Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.970G>A
  hgvsp: ENSP00000347699.6:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.970G>A
  hgvsp: ENSP00000385243.2:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.970G>A
  hgvsp: ENSP00000450858.1:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.970G>A
  hgvsp: ENSP00000451855.1:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.763G>A
  hgvsp: ENSP00000412144.2:p.Glu255Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.970G>A
  hgvsp: ENSP00000383953.2:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.970G>A
  hgvsp: ENSP00000452331.1:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.553G>A
  hgvsp: ENSP00000451912.1:p.Glu185Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.970G>A
  hgvsp: ENSP00000450936.1:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.970G>A
  hgvsp: ENSP00000384218.4:p.Glu324Lys
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu324Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

14-72976875-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976875
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976875
    reference: chr 14
allele count: 1
allele frequency: 8.511072905850511e-6
allele num: 117494
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.979C>G
  hgvsp: ENSP00000450858.1:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.979C>G
  hgvsp: ENSP00000451030.1:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.979C>G
  hgvsp: ENSP00000452331.1:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.979C>G
  hgvsp: ENSP00000384612.4:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.979C>G
  hgvsp: ENSP00000384218.4:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.979C>G
  hgvsp: ENSP00000383953.2:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.979C>G
  hgvsp: ENSP00000385243.2:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.562C>G
  hgvsp: ENSP00000451912.1:p.Gln188Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.979C>G
  hgvsp: ENSP00000451855.1:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.979C>G
  hgvsp: ENSP00000347699.6:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.772C>G
  hgvsp: ENSP00000412144.2:p.Gln258Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.868C>G
  hgvsp: ENSP00000341199.6:p.Gln290Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.979C>G
  hgvsp: ENSP00000450936.1:p.Gln327Glu
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7837
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln327Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

14-72976881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976881
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976881
    reference: chr 14
allele count: 1
allele frequency: 8.446659346228567e-6
allele num: 118390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.985C>T
  hgvsp: ENSP00000347699.6:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.874C>T
  hgvsp: ENSP00000341199.6:p.Arg292Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.985C>T
  hgvsp: ENSP00000385243.2:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.985C>T
  hgvsp: ENSP00000452331.1:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.985C>T
  hgvsp: ENSP00000451855.1:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.985C>T
  hgvsp: ENSP00000450936.1:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.985C>T
  hgvsp: ENSP00000383953.2:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.985C>T
  hgvsp: ENSP00000450858.1:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.985C>T
  hgvsp: ENSP00000384218.4:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.985C>T
  hgvsp: ENSP00000384612.4:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.778C>T
  hgvsp: ENSP00000412144.2:p.Arg260Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.568C>T
  hgvsp: ENSP00000451912.1:p.Arg190Ter
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.985C>T
  hgvsp: ENSP00000451030.1:p.Arg329Ter
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg329Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

14-72976882-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976882
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976882
    reference: chr 14
allele count: 4
allele frequency: 3.370464618547667e-5
allele num: 118678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.986G>A
  hgvsp: ENSP00000450858.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.986G>A
  hgvsp: ENSP00000383953.2:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.986G>A
  hgvsp: ENSP00000450936.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.986G>A
  hgvsp: ENSP00000384612.4:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.986G>A
  hgvsp: ENSP00000347699.6:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.779G>A
  hgvsp: ENSP00000412144.2:p.Arg260Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.569G>A
  hgvsp: ENSP00000451912.1:p.Arg190Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.875G>A
  hgvsp: ENSP00000341199.6:p.Arg292Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.986G>A
  hgvsp: ENSP00000385243.2:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.986G>A
  hgvsp: ENSP00000384218.4:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.986G>A
  hgvsp: ENSP00000452331.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.986G>A
  hgvsp: ENSP00000451030.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.986G>A
  hgvsp: ENSP00000451855.1:p.Arg329Gln
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3968
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg329Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

14-72976898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976898
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976898
    reference: chr 14
allele count: 2
allele frequency: 1.665084836072398e-5
allele num: 120114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1002C>T
  hgvsp: ENST00000554474.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1002C>T
  hgvsp: ENST00000404301.2:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1002C>T
  hgvsp: ENST00000553525.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1002C>T
  hgvsp: ENST00000555571.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1002C>T
  hgvsp: ENST00000406236.4:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1002C>T
  hgvsp: ENST00000407322.4:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1002C>T
  hgvsp: ENST00000556437.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1002C>T
  hgvsp: ENST00000402788.2:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.795C>T
  hgvsp: ENST00000434263.2:c.795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.891C>T
  hgvsp: ENST00000343854.6:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1002C>T
  hgvsp: ENST00000355512.6:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.585C>T
  hgvsp: ENST00000554782.1:c.585C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1002C>T
  hgvsp: ENST00000553530.1:c.1002C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly334Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

14-72976907-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976907
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976907
    reference: chr 14
allele count: 2
allele frequency: 1.658649859014762e-5
allele num: 120580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1011C>T
  hgvsp: ENST00000555571.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1011C>T
  hgvsp: ENST00000406236.4:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1011C>T
  hgvsp: ENST00000404301.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1011C>T
  hgvsp: ENST00000553525.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1011C>T
  hgvsp: ENST00000553530.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1011C>T
  hgvsp: ENST00000407322.4:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.900C>T
  hgvsp: ENST00000343854.6:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.594C>T
  hgvsp: ENST00000554782.1:c.594C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1011C>T
  hgvsp: ENST00000556437.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1011C>T
  hgvsp: ENST00000355512.6:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1011C>T
  hgvsp: ENST00000402788.2:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.804C>T
  hgvsp: ENST00000434263.2:c.804C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1011C>T
  hgvsp: ENST00000554474.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3969
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe337Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

14-72976909-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976909
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976909
    reference: chr 14
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1013A>G
  hgvsp: ENSP00000450936.1:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1013A>G
  hgvsp: ENSP00000347699.6:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1013A>G
  hgvsp: ENSP00000450858.1:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1013A>G
  hgvsp: ENSP00000452331.1:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1013A>G
  hgvsp: ENSP00000451030.1:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1013A>G
  hgvsp: ENSP00000383953.2:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1013A>G
  hgvsp: ENSP00000384218.4:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1013A>G
  hgvsp: ENSP00000385243.2:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1013A>G
  hgvsp: ENSP00000451855.1:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.902A>G
  hgvsp: ENSP00000341199.6:p.Asp301Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1013A>G
  hgvsp: ENSP00000384612.4:p.Asp338Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.596A>G
  hgvsp: ENSP00000451912.1:p.Asp199Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.806A>G
  hgvsp: ENSP00000412144.2:p.Asp269Gly
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7831
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp338Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

14-72976936-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976936
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976936
    reference: chr 14
allele count: 32
allele frequency: 2.64196430045739e-4
allele num: 121122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.929G>A
  hgvsp: ENSP00000341199.6:p.Arg310Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1040G>A
  hgvsp: ENSP00000452331.1:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.623G>A
  hgvsp: ENSP00000451912.1:p.Arg208Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1040G>A
  hgvsp: ENSP00000384218.4:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1040G>A
  hgvsp: ENSP00000385243.2:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.833G>A
  hgvsp: ENSP00000412144.2:p.Arg278Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1040G>A
  hgvsp: ENSP00000450936.1:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1040G>A
  hgvsp: ENSP00000384612.4:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1040G>A
  hgvsp: ENSP00000451030.1:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1040G>A
  hgvsp: ENSP00000347699.6:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1040G>A
  hgvsp: ENSP00000450858.1:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1040G>A
  hgvsp: ENSP00000383953.2:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1040G>A
  hgvsp: ENSP00000451855.1:p.Arg347Gln
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3971
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4705
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg347Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS

14-72976946-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976946
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976946
    reference: chr 14
allele count: 4
allele frequency: 3.300275573010346e-5
allele num: 121202
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1050T>C
  hgvsp: ENST00000355512.6:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1050T>C
  hgvsp: ENST00000553530.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.939T>C
  hgvsp: ENST00000343854.6:c.939T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.843T>C
  hgvsp: ENST00000434263.2:c.843T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.633T>C
  hgvsp: ENST00000554782.1:c.633T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1050T>C
  hgvsp: ENST00000402788.2:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1050T>C
  hgvsp: ENST00000407322.4:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1050T>C
  hgvsp: ENST00000554474.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1050T>C
  hgvsp: ENST00000406236.4:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1050T>C
  hgvsp: ENST00000556437.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1050T>C
  hgvsp: ENST00000553525.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1050T>C
  hgvsp: ENST00000404301.2:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1050T>C
  hgvsp: ENST00000555571.1:c.1050T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe350Phe
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

14-72976951-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976951
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976951
    reference: chr 14
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1055G>A
  hgvsp: ENSP00000450858.1:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1055G>A
  hgvsp: ENSP00000451855.1:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.848G>A
  hgvsp: ENSP00000412144.2:p.Arg283Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1055G>A
  hgvsp: ENSP00000385243.2:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1055G>A
  hgvsp: ENSP00000384218.4:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1055G>A
  hgvsp: ENSP00000383953.2:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1055G>A
  hgvsp: ENSP00000452331.1:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1055G>A
  hgvsp: ENSP00000347699.6:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1055G>A
  hgvsp: ENSP00000384612.4:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1055G>A
  hgvsp: ENSP00000451030.1:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.638G>A
  hgvsp: ENSP00000451912.1:p.Arg213Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.944G>A
  hgvsp: ENSP00000341199.6:p.Arg315Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1055G>A
  hgvsp: ENSP00000450936.1:p.Arg352Gln
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5333
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg352Gln
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

14-72976992-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976992
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976992
    reference: chr 14
allele count: 11
allele frequency: 9.07665648980939e-5
allele num: 121190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+5A>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7804
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1091+5A>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-72976993-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976993
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976993
    reference: chr 14
allele count: 3
allele frequency: 2.475737769855417e-5
allele num: 121176
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+6T>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1091+6T>A
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

14-72976994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72976994
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72976994
    reference: chr 14
allele count: 1
allele frequency: 8.252595441266279e-6
allele num: 121174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+7C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+7C>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4393
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2990
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1091+7C>T
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

14-72977002-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977002
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977002
    reference: chr 14
allele count: 35
allele frequency: 2.888837531777213e-4
allele num: 121156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+15G>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 9.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4395
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5336
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

14-72977006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977006
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977006
    reference: chr 14
allele count: 2
allele frequency: 1.650900566258894e-5
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+19G>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7770
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

14-72977017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977017
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977017
    reference: chr 14
allele count: 10
allele frequency: 8.257365570088519e-5
allele num: 121104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+30G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+30G>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4713
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7769
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/14-72977020-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977020
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977020
    reference: chr 14
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+33A>C
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+33A>C
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3974
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

14-72977021-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977021
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977021
    reference: chr 14
allele count: 8
allele frequency: 6.606656206127674e-5
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+34T>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-72977024-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977024
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977024
    reference: chr 14
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+37G>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3975
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

14-72977025-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977025
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977025
    reference: chr 14
allele count: 5
allele frequency: 4.129774018765693e-5
allele num: 121072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+38T>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4397
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7765
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4714
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

14-72977030-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72977030
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72977030
    reference: chr 14
allele count: 4
allele frequency: 3.304856486607069e-5
allele num: 121034
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.884+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.980+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.674+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1091+43A>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7764
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

14-72983505-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72983505
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72983505
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 32
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-1554G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-1554G>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

14-72983594-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72983594
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72983594
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 8
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-1465C>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum

14-72985013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985013
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985013
    reference: chr 14
allele count: 4
allele frequency: 3.413085770845421e-5
allele num: 117196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-46G>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

14-72985018-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985018
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985018
    reference: chr 14
allele count: 1
allele frequency: 8.517742457539054e-6
allele num: 117402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-41T>G
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-72985022-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985022
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985022
    reference: chr 14
allele count: 3
allele frequency: 2.556847236900419e-5
allele num: 117332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-37C>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23956
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-72985023-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985023
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985023
    reference: chr 14
allele count: 1
allele frequency: 8.507886811073865e-6
allele num: 117538
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-36C>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

14-72985023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985023
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985023
    reference: chr 14
allele count: 1
allele frequency: 8.507886811073865e-6
allele num: 117538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-36C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-36C>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11714
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

14-72985034-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985034
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985034
    reference: chr 14
allele count: 1
allele frequency: 8.438818565400844e-6
allele num: 118500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-25G>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

14-72985036-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985036
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985034
    reference: chr 14
allele count: 1
allele frequency: 8.429428821903027e-6
allele num: 118632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-19_885-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-19_981-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-19_1092-18delGT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-19_675-18delGT
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: CTG
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

14-72985040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985040
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985040
    reference: chr 14
allele count: 1
allele frequency: 8.405480373203328e-6
allele num: 118970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-19G>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

14-72985040-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985040
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985039
    reference: chr 14
allele count: 1
allele frequency: 8.405480373203328e-6
allele num: 118970
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-16delT
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: GT
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

14-72985047-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985047
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985047
    reference: chr 14
allele count: 1
allele frequency: 8.362043014349267e-6
allele num: 119588
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-12C>T
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24800
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/14-72985049-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985049
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985049
    reference: chr 14
allele count: 1
allele frequency: 8.345434212942099e-6
allele num: 119826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.981-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.885-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.675-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1092-10C>A
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

14-72985062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985062
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985062
    reference: chr 14
allele count: 1
allele frequency: 8.28363154406892e-6
allele num: 120720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.888C>T
  hgvsp: ENST00000434263.2:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1095C>T
  hgvsp: ENST00000355512.6:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1095C>T
  hgvsp: ENST00000553530.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1095C>T
  hgvsp: ENST00000407322.4:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1095C>T
  hgvsp: ENST00000555571.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1095C>T
  hgvsp: ENST00000406236.4:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1095C>T
  hgvsp: ENST00000554474.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1095C>T
  hgvsp: ENST00000402788.2:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1095C>T
  hgvsp: ENST00000553525.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.984C>T
  hgvsp: ENST00000343854.6:c.984C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.678C>T
  hgvsp: ENST00000554782.1:c.678C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1095C>T
  hgvsp: ENST00000556437.1:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1095C>T
  hgvsp: ENST00000404301.2:c.1095C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe365Phe
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

14-72985071-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985071
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985071
    reference: chr 14
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1104T>C
  hgvsp: ENST00000406236.4:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1104T>C
  hgvsp: ENST00000407322.4:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1104T>C
  hgvsp: ENST00000554474.1:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1104T>C
  hgvsp: ENST00000402788.2:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.993T>C
  hgvsp: ENST00000343854.6:c.993T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1104T>C
  hgvsp: ENST00000553525.1:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1104T>C
  hgvsp: ENST00000555571.1:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1104T>C
  hgvsp: ENST00000556437.1:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.687T>C
  hgvsp: ENST00000554782.1:c.687T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1104T>C
  hgvsp: ENST00000404301.2:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1104T>C
  hgvsp: ENST00000355512.6:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1104T>C
  hgvsp: ENST00000553530.1:c.1104T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.897T>C
  hgvsp: ENST00000434263.2:c.897T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala368Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

14-72985073-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985073
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985073
    reference: chr 14
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.995T>G
  hgvsp: ENSP00000341199.6:p.Val332Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1106T>G
  hgvsp: ENSP00000385243.2:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1106T>G
  hgvsp: ENSP00000383953.2:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1106T>G
  hgvsp: ENSP00000384612.4:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1106T>G
  hgvsp: ENSP00000451855.1:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.899T>G
  hgvsp: ENSP00000412144.2:p.Val300Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.689T>G
  hgvsp: ENSP00000451912.1:p.Val230Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1106T>G
  hgvsp: ENSP00000450936.1:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1106T>G
  hgvsp: ENSP00000452331.1:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1106T>G
  hgvsp: ENSP00000347699.6:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1106T>G
  hgvsp: ENSP00000384218.4:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1106T>G
  hgvsp: ENSP00000450858.1:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1106T>G
  hgvsp: ENSP00000451030.1:p.Val369Gly
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val369Gly
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

14-72985074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985074
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985074
    reference: chr 14
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1107C>T
  hgvsp: ENST00000556437.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1107C>T
  hgvsp: ENST00000407322.4:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.690C>T
  hgvsp: ENST00000554782.1:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1107C>T
  hgvsp: ENST00000554474.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1107C>T
  hgvsp: ENST00000406236.4:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1107C>T
  hgvsp: ENST00000402788.2:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1107C>T
  hgvsp: ENST00000355512.6:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.900C>T
  hgvsp: ENST00000434263.2:c.900C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.996C>T
  hgvsp: ENST00000343854.6:c.996C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1107C>T
  hgvsp: ENST00000555571.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1107C>T
  hgvsp: ENST00000404301.2:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1107C>T
  hgvsp: ENST00000553525.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1107C>T
  hgvsp: ENST00000553530.1:c.1107C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val369Val
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/14-72985084-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985084
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985084
    reference: chr 14
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.700A>C
  hgvsp: ENSP00000451912.1:p.Lys234Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1117A>C
  hgvsp: ENSP00000450858.1:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1117A>C
  hgvsp: ENSP00000385243.2:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1117A>C
  hgvsp: ENSP00000383953.2:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1117A>C
  hgvsp: ENSP00000450936.1:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1006A>C
  hgvsp: ENSP00000341199.6:p.Lys336Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.910A>C
  hgvsp: ENSP00000412144.2:p.Lys304Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1117A>C
  hgvsp: ENSP00000451030.1:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1117A>C
  hgvsp: ENSP00000452331.1:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1117A>C
  hgvsp: ENSP00000384218.4:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1117A>C
  hgvsp: ENSP00000384612.4:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1117A>C
  hgvsp: ENSP00000347699.6:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1117A>C
  hgvsp: ENSP00000451855.1:p.Lys373Gln
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11949
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys373Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/14-72985090-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985090
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985090
    reference: chr 14
allele count: 7
allele frequency: 5.770911309337334e-5
allele num: 121298
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1123C>A
  hgvsp: ENSP00000450936.1:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.916C>A
  hgvsp: ENSP00000412144.2:p.Gln306Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.706C>A
  hgvsp: ENSP00000451912.1:p.Gln236Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1123C>A
  hgvsp: ENSP00000451030.1:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1123C>A
  hgvsp: ENSP00000384218.4:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1123C>A
  hgvsp: ENSP00000452331.1:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1123C>A
  hgvsp: ENSP00000451855.1:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1123C>A
  hgvsp: ENSP00000347699.6:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1123C>A
  hgvsp: ENSP00000384612.4:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1123C>A
  hgvsp: ENSP00000385243.2:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1123C>A
  hgvsp: ENSP00000383953.2:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1012C>A
  hgvsp: ENSP00000341199.6:p.Gln338Lys
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1123C>A
  hgvsp: ENSP00000450858.1:p.Gln375Lys
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13250
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11956
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln375Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

14-72985096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985096
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985096
    reference: chr 14
allele count: 2
allele frequency: 1.648396933981703e-5
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1129C>T
  hgvsp: ENST00000406236.4:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1129C>T
  hgvsp: ENST00000556437.1:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1129C>T
  hgvsp: ENST00000553525.1:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1129C>T
  hgvsp: ENST00000407322.4:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.922C>T
  hgvsp: ENST00000434263.2:c.922C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1129C>T
  hgvsp: ENST00000553530.1:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1129C>T
  hgvsp: ENST00000404301.2:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1129C>T
  hgvsp: ENST00000355512.6:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1129C>T
  hgvsp: ENST00000554474.1:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1018C>T
  hgvsp: ENST00000343854.6:c.1018C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.712C>T
  hgvsp: ENST00000554782.1:c.712C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1129C>T
  hgvsp: ENST00000555571.1:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1129C>T
  hgvsp: ENST00000402788.2:c.1129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu377Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

14-72985098-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985098
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985098
    reference: chr 14
allele count: 2
allele frequency: 1.648288252649623e-5
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1131A>G
  hgvsp: ENST00000406236.4:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.714A>G
  hgvsp: ENST00000554782.1:c.714A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1131A>G
  hgvsp: ENST00000555571.1:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1131A>G
  hgvsp: ENST00000355512.6:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1131A>G
  hgvsp: ENST00000407322.4:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1131A>G
  hgvsp: ENST00000402788.2:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1131A>G
  hgvsp: ENST00000554474.1:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1131A>G
  hgvsp: ENST00000553530.1:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1020A>G
  hgvsp: ENST00000343854.6:c.1020A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1131A>G
  hgvsp: ENST00000404301.2:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1131A>G
  hgvsp: ENST00000556437.1:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.924A>G
  hgvsp: ENST00000434263.2:c.924A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1131A>G
  hgvsp: ENST00000553525.1:c.1131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu377Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

14-72985098-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985098
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985098
    reference: chr 14
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1131A>T
  hgvsp: ENST00000553525.1:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1020A>T
  hgvsp: ENST00000343854.6:c.1020A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1131A>T
  hgvsp: ENST00000404301.2:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1131A>T
  hgvsp: ENST00000407322.4:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1131A>T
  hgvsp: ENST00000355512.6:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1131A>T
  hgvsp: ENST00000556437.1:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1131A>T
  hgvsp: ENST00000554474.1:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1131A>T
  hgvsp: ENST00000553530.1:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.924A>T
  hgvsp: ENST00000434263.2:c.924A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1131A>T
  hgvsp: ENST00000406236.4:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1131A>T
  hgvsp: ENST00000402788.2:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.714A>T
  hgvsp: ENST00000554782.1:c.714A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1131A>T
  hgvsp: ENST00000555571.1:c.1131A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3829
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu377Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

14-72985104-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985104
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985104
    reference: chr 14
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1137T>A
  hgvsp: ENSP00000450936.1:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1137T>A
  hgvsp: ENSP00000384612.4:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1137T>A
  hgvsp: ENSP00000450858.1:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1137T>A
  hgvsp: ENSP00000385243.2:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1026T>A
  hgvsp: ENSP00000341199.6:p.Asp342Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1137T>A
  hgvsp: ENSP00000384218.4:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1137T>A
  hgvsp: ENSP00000383953.2:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1137T>A
  hgvsp: ENSP00000451030.1:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1137T>A
  hgvsp: ENSP00000452331.1:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1137T>A
  hgvsp: ENSP00000347699.6:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.930T>A
  hgvsp: ENSP00000412144.2:p.Asp310Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.720T>A
  hgvsp: ENSP00000451912.1:p.Asp240Glu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1137T>A
  hgvsp: ENSP00000451855.1:p.Asp379Glu
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp379Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

14-72985104-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985104
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985104
    reference: chr 14
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.720T>C
  hgvsp: ENST00000554782.1:c.720T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1137T>C
  hgvsp: ENST00000402788.2:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1137T>C
  hgvsp: ENST00000554474.1:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1137T>C
  hgvsp: ENST00000404301.2:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1026T>C
  hgvsp: ENST00000343854.6:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1137T>C
  hgvsp: ENST00000555571.1:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1137T>C
  hgvsp: ENST00000553530.1:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1137T>C
  hgvsp: ENST00000407322.4:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1137T>C
  hgvsp: ENST00000406236.4:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1137T>C
  hgvsp: ENST00000553525.1:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1137T>C
  hgvsp: ENST00000355512.6:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.930T>C
  hgvsp: ENST00000434263.2:c.930T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1137T>C
  hgvsp: ENST00000556437.1:c.1137T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp379Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

14-72985108-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985108
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985108
    reference: chr 14
allele count: 4
allele frequency: 3.296033224014898e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1141G>T
  hgvsp: ENSP00000451030.1:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1141G>T
  hgvsp: ENSP00000384218.4:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1141G>T
  hgvsp: ENSP00000450858.1:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1141G>T
  hgvsp: ENSP00000347699.6:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.934G>T
  hgvsp: ENSP00000412144.2:p.Ala312Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1141G>T
  hgvsp: ENSP00000383953.2:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1030G>T
  hgvsp: ENSP00000341199.6:p.Ala344Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1141G>T
  hgvsp: ENSP00000451855.1:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1141G>T
  hgvsp: ENSP00000385243.2:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1141G>T
  hgvsp: ENSP00000450936.1:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.724G>T
  hgvsp: ENSP00000451912.1:p.Ala242Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1141G>T
  hgvsp: ENSP00000384612.4:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1141G>T
  hgvsp: ENSP00000452331.1:p.Ala381Ser
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala381Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

14-72985117-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985117
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985117
    reference: chr 14
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1150G>A
  hgvsp: ENSP00000384612.4:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1150G>A
  hgvsp: ENSP00000452331.1:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1150G>A
  hgvsp: ENSP00000450858.1:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1039G>A
  hgvsp: ENSP00000341199.6:p.Val347Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1150G>A
  hgvsp: ENSP00000451030.1:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1150G>A
  hgvsp: ENSP00000451855.1:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.733G>A
  hgvsp: ENSP00000451912.1:p.Val245Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1150G>A
  hgvsp: ENSP00000450936.1:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.943G>A
  hgvsp: ENSP00000412144.2:p.Val315Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1150G>A
  hgvsp: ENSP00000347699.6:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1150G>A
  hgvsp: ENSP00000383953.2:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1150G>A
  hgvsp: ENSP00000384218.4:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1150G>A
  hgvsp: ENSP00000385243.2:p.Val384Ile
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val384Ile
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

14-72985117-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72985117
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 72985117
    reference: chr 14
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000412144
  ensembl transcript: ENST00000434263
  gene symbol: RGS6
  hgvsc: ENST00000434263.2:c.943G>T
  hgvsp: ENSP00000412144.2:p.Val315Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450858
  ensembl transcript: ENST00000554474
  gene symbol: RGS6
  hgvsc: ENST00000554474.1:c.1150G>T
  hgvsp: ENSP00000450858.1:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384612
  ensembl transcript: ENST00000407322
  gene symbol: RGS6
  hgvsc: ENST00000407322.4:c.1150G>T
  hgvsp: ENSP00000384612.4:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451855
  ensembl transcript: ENST00000556437
  gene symbol: RGS6
  hgvsc: ENST00000556437.1:c.1150G>T
  hgvsp: ENSP00000451855.1:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000452331
  ensembl transcript: ENST00000553530
  gene symbol: RGS6
  hgvsc: ENST00000553530.1:c.1150G>T
  hgvsp: ENSP00000452331.1:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000384218
  ensembl transcript: ENST00000406236
  gene symbol: RGS6
  hgvsc: ENST00000406236.4:c.1150G>T
  hgvsp: ENSP00000384218.4:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000341199
  ensembl transcript: ENST00000343854
  gene symbol: RGS6
  hgvsc: ENST00000343854.6:c.1039G>T
  hgvsp: ENSP00000341199.6:p.Val347Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000383953
  ensembl transcript: ENST00000402788
  gene symbol: RGS6
  hgvsc: ENST00000402788.2:c.1150G>T
  hgvsp: ENSP00000383953.2:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451030
  ensembl transcript: ENST00000553525
  gene symbol: RGS6
  hgvsc: ENST00000553525.1:c.1150G>T
  hgvsp: ENSP00000451030.1:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000347699
  ensembl transcript: ENST00000355512
  gene symbol: RGS6
  hgvsc: ENST00000355512.6:c.1150G>T
  hgvsp: ENSP00000347699.6:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000385243
  ensembl transcript: ENST00000404301
  gene symbol: RGS6
  hgvsc: ENST00000404301.2:c.1150G>T
  hgvsp: ENSP00000385243.2:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000451912
  ensembl transcript: ENST00000554782
  gene symbol: RGS6
  hgvsc: ENST00000554782.1:c.733G>T
  hgvsp: ENSP00000451912.1:p.Val245Leu
  variant of: http://identifiers.org/hgnc/10002
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182732
  ensembl protein: ENSP00000450936
  ensembl transcript: ENST00000555571
  gene symbol: RGS6
  hgvsc: ENST00000555571.1:c.1150G>T
  hgvsp: ENSP00000450936.1:p.Val384Leu
  variant of: http://identifiers.org/hgnc/10002
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25750
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val384Leu
num of homozygotes: 0
population: European (Non-Finnish)
reference allele: G

GenotypeDepth
all individuals: 10052
bin: 3.25e1
variant carriers: 3

GenotypeDepth
all individuals: 507
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 5238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2252
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3591
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3461
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22530
bin: 9.75e1
variant carriers: 72

GenotypeQuality
all individuals: 10786
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7258
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4599
bin: 8.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 72
allele frequency: 4.363636363636364e-3
allele num: 16500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.857e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e0

DP
type: SiteQuality
SIO_000300: 2.797509e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

QD
type: SiteQuality
SIO_000300: 1.363e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeDepth
all individuals: 8602
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3141
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 579
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3594
bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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East Asian
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Latino
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InbreedingCoeff
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DP
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MQRankSum
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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African
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European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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VQSLOD
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QD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Finnish)
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East Asian
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African
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Latino
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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QD
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MQ
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DP
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Other
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ReadPosRankSum
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FS
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Finnish)
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European (Non-Finnish)
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South Asian
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Latino
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East Asian
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African
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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Other
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BaseQRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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DP
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VQSLOD
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Other
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African
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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BaseQRankSum
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QD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6592
num of homozygotes: 0

Other
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10008
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.560305819940709e-5
allele num: 64090
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.22e0

MQ
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SIO_000300: 5.929e1

VQSLOD
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DP
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InbreedingCoeff
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QD
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FS
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BaseQRankSum
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SIO_000300: 1.55e0

ClippingRankSum
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SIO_000300: -1.13e-1

ReadPosRankSum
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SIO_000300: 3.4e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8472
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.992006394884092e-5
allele num: 10008
num of homozygotes: 0

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

Other
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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 count: 0
allele frequency: 0.0e0
allele num: 64102
num of homozygotes: 0

Latino
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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DP
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VQSLOD
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MQ
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.559673092519808e-5
allele num: 64116
num of homozygotes: 0

Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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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

South Asian
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BaseQRankSum
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SIO_000300: 2.9e0

MQ
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SIO_000300: 5.893e1

InbreedingCoeff
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SIO_000300: -1.9e-3

QD
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FS
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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SIO_000300: -1.58e-1

MQRankSum
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SIO_000300: -3.2e-1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64124
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
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
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allele count: 1
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allele num: 10016
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

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

InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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DP
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MQ
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SIO_000300: 5.886e1

FS
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SIO_000300: 4.617e0

ClippingRankSum
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SIO_000300: -1.718e0

ReadPosRankSum
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SIO_000300: 1.38e0

MQRankSum
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SIO_000300: -1.238e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

Other
type: Population
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African
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East Asian
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.113906707355048e-5
allele num: 64228
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.52e-1

MQ
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.75e1
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

African
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allele num: 10060
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East Asian
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Other
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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DP
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MQRankSum
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6592
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
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African
type: Population
allele count: 0
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Latino
type: Population
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allele frequency: 8.721437292865864e-5
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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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.548227279764669e-5
allele num: 64590
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FS
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BaseQRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -3.65e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 26
allele frequency: 2.574257425742574e-3
allele num: 10100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 8.719916288803627e-5
allele num: 11468
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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
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

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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QD
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SIO_000300: 1.221e1

DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65000
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Other
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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

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

ReadPosRankSum
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SIO_000300: 7.11e-1

VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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MQRankSum
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BaseQRankSum
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SIO_000300: 5.79e0

DP
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SIO_000300: 3.9362e6

FS
type: SiteQuality
SIO_000300: 4.957e0

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65330
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

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

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

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

ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.9e-3

MQ
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SIO_000300: 5.652e1

FS
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 9.775171065493646e-5
allele num: 10230
num of homozygotes: 0

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

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

Other
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South Asian
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Latino
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allele frequency: 0.0e0
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QD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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Other
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European (Finnish)
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allele frequency: 0.0e0
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14802
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.028284174186906e-5
allele num: 66044
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.950458357714063e-4
allele num: 10254
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 5.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ReadPosRankSum
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SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

DP
type: SiteQuality
SIO_000300: 3.975378e6

QD
type: SiteQuality
SIO_000300: 1.183e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 666
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15822
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506704836522525e-5
allele num: 66370
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.718172983479106e-5
allele num: 10290
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.989e1

VQSLOD
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SIO_000300: 1.65e0

DP
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SIO_000300: 3.991428e6

InbreedingCoeff
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SIO_000300: -3.0e-4

BaseQRankSum
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SIO_000300: -4.766e0

QD
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SIO_000300: 1.285e1

FS
type: SiteQuality
SIO_000300: 5.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ClippingRankSum
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SIO_000300: 1.26e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.008604609182261e-5
allele num: 66476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

VQSLOD
type: SiteQuality
SIO_000300: -6.719000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
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SIO_000300: 5.905e1

FS
type: SiteQuality
SIO_000300: 2.116e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.186e1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.68e-1

DP
type: SiteQuality
SIO_000300: 3.998146e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2024
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503262078710802e-5
allele num: 66522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

BaseQRankSum
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SIO_000300: 6.27e0

ReadPosRankSum
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SIO_000300: 8.44e-1

QD
type: SiteQuality
SIO_000300: 1.526e1

FS
type: SiteQuality
SIO_000300: 1.726e0

DP
type: SiteQuality
SIO_000300: 3.999851e6

VQSLOD
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
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SIO_000300: -1.222e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 29

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6610
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.935359009096187e-4
allele num: 10334
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596503375454388e-4
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.052715319263907e-4
allele num: 66622
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
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.98e-1

VQSLOD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
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SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.371e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 4.008243e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500330072615976e-5
allele num: 66652
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.595155709342561e-4
allele num: 11560
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
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QD
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
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SIO_000300: -9.93e-1

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.867e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.650115508085566e-4
allele num: 66662
num of homozygotes: 0

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

Other
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South Asian
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East Asian
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Latino
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allele frequency: 0.0e0
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FS
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BaseQRankSum
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QD
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DP
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
allele num: 906
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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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: 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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Latino
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allele frequency: 2.595155709342561e-4
allele num: 11560
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -1.913e0

InbreedingCoeff
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DP
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ReadPosRankSum
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MQRankSum
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QD
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FS
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MQ
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SIO_000300: 5.975e1

VQSLOD
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ClippingRankSum
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SIO_000300: -1.89e-1

GenotypeDepth
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 11562
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 count: 1
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allele num: 8620
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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VQSLOD
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SIO_000300: -2.387e0

FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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SIO_000300: 3.36e0

DP
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SIO_000300: 3.99929e6

GenotypeDepth
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GenotypeDepth
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variant carriers: 2

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

Latino
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allele frequency: 5.189413596263622e-4
allele num: 11562
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.940993788819876e-4
allele num: 10304
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 27
allele frequency: 4.051255889325691e-4
allele num: 66646
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

European (Non-Finnish)
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allele num: 66642
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South Asian
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Other
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African
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European (Finnish)
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East Asian
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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ReadPosRankSum
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FS
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BaseQRankSum
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

Other
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South Asian
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allele num: 16506
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East Asian
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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DP
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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South Asian
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Latino
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European (Finnish)
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ReadPosRankSum
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FS
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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MQ
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DP
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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DP
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MQ
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European (Non-Finnish)
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East Asian
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African
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South Asian
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MQ
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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GenotypeQuality
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East Asian
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European (Finnish)
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QD
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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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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.526111772426212e-5
allele num: 65526
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South Asian
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African
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Latino
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European (Finnish)
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allele frequency: 4.539951573849879e-4
allele num: 6608
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East Asian
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VQSLOD
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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Other
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European (Non-Finnish)
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East Asian
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African
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South Asian
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FS
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ClippingRankSum
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DP
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MQ
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
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Other
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Latino
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European (Non-Finnish)
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allele num: 65556
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African
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South Asian
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele 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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European (Non-Finnish)
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allele num: 65620
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European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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num of homozygotes: 0

Other
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FS
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SIO_000300: 1.8502e1

MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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East Asian
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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South Asian
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African
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East Asian
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DP
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.63020030816641e-5
allele num: 10384
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East Asian
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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FS
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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Latino
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South Asian
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African
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FS
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ClippingRankSum
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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SIO_000300: 5.915e1

ReadPosRankSum
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BaseQRankSum
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QD
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Latino
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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
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European (Finnish)
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allele count: 0
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Other
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South Asian
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African
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MQRankSum
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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num of homozygotes: 0

European (Non-Finnish)
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South Asian
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Latino
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African
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Other
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European (Finnish)
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InbreedingCoeff
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DP
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BaseQRankSum
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ClippingRankSum
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MQ
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MQRankSum
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QD
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FS
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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InbreedingCoeff
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MQRankSum
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QD
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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African
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European (Non-Finnish)
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Other
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European (Finnish)
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South Asian
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InbreedingCoeff
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MQ
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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QD
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DP
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3647
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.176e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

DP
type: SiteQuality
SIO_000300: 1.819765e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

QD
type: SiteQuality
SIO_000300: 1.343e1

VQSLOD
type: SiteQuality
SIO_000300: 8.139999999999999e-1

GenotypeDepth
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 9.25e1
variant carriers: 1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1775
bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5608
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9110
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2348
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

VQSLOD
type: SiteQuality
SIO_000300: 8.139999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.176e0

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.819765e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

QD
type: SiteQuality
SIO_000300: 1.343e1

GenotypeDepth
all individuals: 1773
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1122
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13271
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3824
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2966
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 964
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5607
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 3648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2349
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9109
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497616263380409e-5
allele num: 66702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.722e0

FS
type: SiteQuality
SIO_000300: 3.311e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

DP
type: SiteQuality
SIO_000300: 1.820065e6

MQRankSum
type: SiteQuality
SIO_000300: 2.97e-1

GenotypeDepth
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1120
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 122
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 667
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 31
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9116
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3652
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5604
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 1.820173e6

MQRankSum
type: SiteQuality
SIO_000300: 1.72e-1

FS
type: SiteQuality
SIO_000300: 6.807e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.068e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.203e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

GenotypeDepth
all individuals: 122
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11961
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1120
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3826
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9116
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3652
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2970
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 5604
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1227
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34612
bin: 6.25e1
variant carriers: 0

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