4-3417900-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3417900
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3417900
    reference: chr 4
allele count: 1
allele frequency: 8.776857182979919e-6
allele num: 113936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1384+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2427+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.453+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.483+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.565+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1493+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.618+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*401+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.621+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2427+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*401+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2427+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.708+52A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.882+52A>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9055
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8201
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-3418599-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418599
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418599
    reference: chr 4
allele count: 13
allele frequency: 1.164415463437354e-4
allele num: 111644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-41G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-41G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

4-3418602-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418602
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418602
    reference: chr 4
allele count: 1
allele frequency: 8.953353030710001e-6
allele num: 111690
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-38C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-38C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

4-3418606-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418606
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418606
    reference: chr 4
allele count: 17
allele frequency: 1.519512325926456e-4
allele num: 111878
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-34C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-34C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

4-3418609-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418609
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418609
    reference: chr 4
allele count: 2
allele frequency: 1.786192730195588e-5
allele num: 111970
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-31G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-31G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

4-3418619-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418619
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418619
    reference: chr 4
allele count: 1
allele frequency: 8.877525656049147e-6
allele num: 112644
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-21C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-21C>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

4-3418622-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418622
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418622
    reference: chr 4
allele count: 1
allele frequency: 8.854572501239641e-6
allele num: 112936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-18C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-18C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

4-3418625-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418625
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418625
    reference: chr 4
allele count: 1
allele frequency: 8.829242450997704e-6
allele num: 113260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-15A>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3617
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

4-3418635-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418635
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418635
    reference: chr 4
allele count: 9
allele frequency: 7.849978194505015e-5
allele num: 114650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2428-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.454-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.709-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2428-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.619-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.883-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*402-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1494-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.484-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2428-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.566-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.622-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*402-5C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1385-5C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21630
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2428-5C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

4-3418645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418645
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418645
    reference: chr 4
allele count: 3
allele frequency: 2.580733960738434e-5
allele num: 116246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.624C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.459C>T
  hgvsp: ENST00000538395.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*407C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.714C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.489C>T
  hgvsp: ENST00000338806.4:c.489C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2433C>T
  hgvsp: ENST00000382788.3:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2433C>T
  hgvsp: ENST00000336727.3:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2433C>T
  hgvsp: ENST00000344733.5:c.2433C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1499C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.888C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.627C>T
  hgvsp: ENST00000306648.7:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.571C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1390C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*407C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe811Phe
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-3418647-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418647
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418647
    reference: chr 4
allele count: 2
allele frequency: 1.715677864324194e-5
allele num: 116572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.716A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2435A>G
  hgvsp: ENSP00000339381.5:p.Asn812Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2435A>G
  hgvsp: ENSP00000372238.3:p.Asn812Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*409A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.461A>G
  hgvsp: ENSP00000438888.1:p.Asn154Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.626A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.629A>G
  hgvsp: ENSP00000304459.7:p.Asn210Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2435A>G
  hgvsp: ENSP00000338509.3:p.Asn812Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.573A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*409A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1501A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.491A>G
  hgvsp: ENSP00000342133.4:p.Asn164Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.890A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1392A>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8173
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn812Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

4-3418660-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418660
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418660
    reference: chr 4
allele count: 1
allele frequency: 8.439958137807636e-6
allele num: 118484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.504T>C
  hgvsp: ENST00000338806.4:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*422T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2448T>C
  hgvsp: ENST00000344733.5:c.2448T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2448T>C
  hgvsp: ENST00000382788.3:c.2448T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.474T>C
  hgvsp: ENST00000538395.1:c.474T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.642T>C
  hgvsp: ENST00000306648.7:c.642T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2448T>C
  hgvsp: ENST00000336727.3:c.2448T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*422T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1405T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.903T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.729T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.586T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1514T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.639T>C
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe816Phe
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

4-3418669-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418669
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418669
    reference: chr 4
allele count: 5
allele frequency: 4.180532098125449e-5
allele num: 119602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.513C>T
  hgvsp: ENST00000338806.4:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2457C>T
  hgvsp: ENST00000382788.3:c.2457C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1414C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.595C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.483C>T
  hgvsp: ENST00000538395.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.651C>T
  hgvsp: ENST00000306648.7:c.651C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.738C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2457C>T
  hgvsp: ENST00000336727.3:c.2457C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.912C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2457C>T
  hgvsp: ENST00000344733.5:c.2457C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*431C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1523C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.648C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*431C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr819Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/4-3418682-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418682
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418682
    reference: chr 4
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2470A>C
  hgvsp: ENSP00000339381.5:p.Lys824Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.608A>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.664A>C
  hgvsp: ENSP00000304459.7:p.Lys222Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.526A>C
  hgvsp: ENSP00000342133.4:p.Lys176Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.496A>C
  hgvsp: ENSP00000438888.1:p.Lys166Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*444A>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1536A>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2470A>C
  hgvsp: ENSP00000338509.3:p.Lys824Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.751A>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.925A>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2470A>C
  hgvsp: ENSP00000372238.3:p.Lys824Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*444A>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.661A>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1427A>C
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10054
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18480
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys824Gln
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD

4-3418689-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418689
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418689
    reference: chr 4
allele count: 1
allele frequency: 8.293524416135881e-6
allele num: 120576
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2477C>T
  hgvsp: ENSP00000339381.5:p.Pro826Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1434C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2477C>T
  hgvsp: ENSP00000338509.3:p.Pro826Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.758C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.615C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2477C>T
  hgvsp: ENSP00000372238.3:p.Pro826Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.671C>T
  hgvsp: ENSP00000304459.7:p.Pro224Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.533C>T
  hgvsp: ENSP00000342133.4:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1543C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.932C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.503C>T
  hgvsp: ENSP00000438888.1:p.Pro168Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.668C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*451C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*451C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro826Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-3418693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418693
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418693
    reference: chr 4
allele count: 2
allele frequency: 1.658017342861406e-5
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.936G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*455G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2481G>A
  hgvsp: ENST00000336727.3:c.2481G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2481G>A
  hgvsp: ENST00000382788.3:c.2481G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.537G>A
  hgvsp: ENST00000338806.4:c.537G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.619G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.675G>A
  hgvsp: ENST00000306648.7:c.675G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2481G>A
  hgvsp: ENST00000344733.5:c.2481G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.762G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.672G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*455G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1547G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.507G>A
  hgvsp: ENST00000538395.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1438G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu827Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-3418713-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418713
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418713
    reference: chr 4
allele count: 4
allele frequency: 3.316309610665252e-5
allele num: 120616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2501C>T
  hgvsp: ENSP00000338509.3:p.Ala834Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.956C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2501C>T
  hgvsp: ENSP00000372238.3:p.Ala834Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2501C>T
  hgvsp: ENSP00000339381.5:p.Ala834Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.639C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*475C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.782C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.527C>T
  hgvsp: ENSP00000438888.1:p.Ala176Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*475C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.557C>T
  hgvsp: ENSP00000342133.4:p.Ala186Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.695C>T
  hgvsp: ENSP00000304459.7:p.Ala232Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1458C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1567C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.692C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ala834Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-3418714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418714
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418714
    reference: chr 4
allele count: 269
allele frequency: 2.230884060374855e-3
allele num: 120580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*476G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*476G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2502G>A
  hgvsp: ENST00000336727.3:c.2502G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.558G>A
  hgvsp: ENST00000338806.4:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.783G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.640G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2502G>A
  hgvsp: ENST00000344733.5:c.2502G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1568G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.696G>A
  hgvsp: ENST00000306648.7:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2502G>A
  hgvsp: ENST00000382788.3:c.2502G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.957G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.528G>A
  hgvsp: ENST00000538395.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1459G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.693G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 6409
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18472
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
hgvs: p.Ala834Ala
num of homozygotes: 2
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-3418724-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418724
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418724
    reference: chr 4
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2512G>A
  hgvsp: ENSP00000372238.3:p.Gly838Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2512G>A
  hgvsp: ENSP00000339381.5:p.Gly838Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1469G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2512G>A
  hgvsp: ENSP00000338509.3:p.Gly838Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.538G>A
  hgvsp: ENSP00000438888.1:p.Gly180Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*486G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.568G>A
  hgvsp: ENSP00000342133.4:p.Gly190Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.703G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.706G>A
  hgvsp: ENSP00000304459.7:p.Gly236Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.793G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*486G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1578G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.650G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.967G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22897
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly838Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

4-3418725-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418725
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418725
    reference: chr 4
allele count: 1
allele frequency: 8.296827293243064e-6
allele num: 120528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*487G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.704G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1470G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.539G>T
  hgvsp: ENSP00000438888.1:p.Gly180Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*487G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.651G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2513G>T
  hgvsp: ENSP00000372238.3:p.Gly838Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2513G>T
  hgvsp: ENSP00000339381.5:p.Gly838Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.707G>T
  hgvsp: ENSP00000304459.7:p.Gly236Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.569G>T
  hgvsp: ENSP00000342133.4:p.Gly190Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.794G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1579G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2513G>T
  hgvsp: ENSP00000338509.3:p.Gly838Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.968G>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly838Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

4-3418726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418726
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418726
    reference: chr 4
allele count: 1
allele frequency: 8.30137304710199e-6
allele num: 120462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2514C>T
  hgvsp: ENST00000336727.3:c.2514C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.708C>T
  hgvsp: ENST00000306648.7:c.708C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.570C>T
  hgvsp: ENST00000338806.4:c.570C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.795C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.969C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*488C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1580C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.705C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2514C>T
  hgvsp: ENST00000382788.3:c.2514C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2514C>T
  hgvsp: ENST00000344733.5:c.2514C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.540C>T
  hgvsp: ENST00000538395.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*488C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.652C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1471C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly838Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff

4-3418727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418727
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418727
    reference: chr 4
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1472C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.970C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2515C>T
  hgvsp: ENSP00000372238.3:p.Arg839Cys
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.706C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.571C>T
  hgvsp: ENSP00000342133.4:p.Arg191Cys
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2515C>T
  hgvsp: ENSP00000338509.3:p.Arg839Cys
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.796C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*489C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.709C>T
  hgvsp: ENSP00000304459.7:p.Arg237Cys
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.541C>T
  hgvsp: ENSP00000438888.1:p.Arg181Cys
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.653C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2515C>T
  hgvsp: ENSP00000339381.5:p.Arg839Cys
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*489C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1581C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9823
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg839Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

4-3418728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418728
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418728
    reference: chr 4
allele count: 2
allele frequency: 1.660384877214538e-5
allele num: 120454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*490G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2516G>A
  hgvsp: ENSP00000339381.5:p.Arg839His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2516G>A
  hgvsp: ENSP00000372238.3:p.Arg839His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2516G>A
  hgvsp: ENSP00000338509.3:p.Arg839His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.797G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.707G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1473G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.654G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.710G>A
  hgvsp: ENSP00000304459.7:p.Arg237His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*490G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.542G>A
  hgvsp: ENSP00000438888.1:p.Arg181His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1582G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.572G>A
  hgvsp: ENSP00000342133.4:p.Arg191His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.971G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg839His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

4-3418737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418737
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418737
    reference: chr 4
allele count: 19
allele frequency: 1.578230388410805e-4
allele num: 120388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.551C>T
  hgvsp: ENSP00000438888.1:p.Pro184Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.980C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2525C>T
  hgvsp: ENSP00000339381.5:p.Pro842Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.806C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1482C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.719C>T
  hgvsp: ENSP00000304459.7:p.Pro240Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2525C>T
  hgvsp: ENSP00000338509.3:p.Pro842Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2525C>T
  hgvsp: ENSP00000372238.3:p.Pro842Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*499C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.663C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*499C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.581C>T
  hgvsp: ENSP00000342133.4:p.Pro194Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1591C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.716C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro842Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

4-3418738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418738
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418738
    reference: chr 4
allele count: 2
allele frequency: 1.661515967168445e-5
allele num: 120372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2526G>A
  hgvsp: ENST00000344733.5:c.2526G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.720G>A
  hgvsp: ENST00000306648.7:c.720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.582G>A
  hgvsp: ENST00000338806.4:c.582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.981G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1592G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1483G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*500G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2526G>A
  hgvsp: ENST00000336727.3:c.2526G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2526G>A
  hgvsp: ENST00000382788.3:c.2526G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*500G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.717G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.807G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.664G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.552G>A
  hgvsp: ENST00000538395.1:c.552G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro842Pro
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

4-3418739-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418739
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418739
    reference: chr 4
allele count: 1
allele frequency: 8.307441806370146e-6
allele num: 120374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.982G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1484G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2527G>T
  hgvsp: ENSP00000338509.3:p.Asp843Tyr
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1593G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.808G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*501G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.583G>T
  hgvsp: ENSP00000342133.4:p.Asp195Tyr
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.721G>T
  hgvsp: ENSP00000304459.7:p.Asp241Tyr
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2527G>T
  hgvsp: ENSP00000339381.5:p.Asp843Tyr
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2527G>T
  hgvsp: ENSP00000372238.3:p.Asp843Tyr
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.665G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.553G>T
  hgvsp: ENSP00000438888.1:p.Asp185Tyr
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*501G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.718G>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp843Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

4-3418740-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418740
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418740
    reference: chr 4
allele count: 5
allele frequency: 4.153858934950569e-5
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1594A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*502A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.809A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2528A>T
  hgvsp: ENSP00000338509.3:p.Asp843Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.584A>T
  hgvsp: ENSP00000342133.4:p.Asp195Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.983A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2528A>T
  hgvsp: ENSP00000372238.3:p.Asp843Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.719A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.554A>T
  hgvsp: ENSP00000438888.1:p.Asp185Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2528A>T
  hgvsp: ENSP00000339381.5:p.Asp843Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.722A>T
  hgvsp: ENSP00000304459.7:p.Asp241Val
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1485A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.666A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*502A>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22874
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp843Val
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: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

4-3418743-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418743
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418743
    reference: chr 4
allele count: 3
allele frequency: 2.493268175925002e-5
allele num: 120324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.587C>T
  hgvsp: ENSP00000342133.4:p.Ser196Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*505C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1597C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2531C>T
  hgvsp: ENSP00000372238.3:p.Ser844Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.557C>T
  hgvsp: ENSP00000438888.1:p.Ser186Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.669C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.986C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*505C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.722C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.725C>T
  hgvsp: ENSP00000304459.7:p.Ser242Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2531C>T
  hgvsp: ENSP00000338509.3:p.Ser844Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1488C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.812C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2531C>T
  hgvsp: ENSP00000339381.5:p.Ser844Leu
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser844Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

4-3418744-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418744
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418744
    reference: chr 4
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1489G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.558G>A
  hgvsp: ENST00000538395.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.723G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2532G>A
  hgvsp: ENST00000382788.3:c.2532G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.588G>A
  hgvsp: ENST00000338806.4:c.588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.813G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.670G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2532G>A
  hgvsp: ENST00000336727.3:c.2532G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*506G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2532G>A
  hgvsp: ENST00000344733.5:c.2532G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*506G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.726G>A
  hgvsp: ENST00000306648.7:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.987G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1598G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser844Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

4-3418744-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418744
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418744
    reference: chr 4
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.670G>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*506G>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.813G>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.726G>C
  hgvsp: ENST00000306648.7:c.726G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2532G>C
  hgvsp: ENST00000336727.3:c.2532G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2532G>C
  hgvsp: ENST00000382788.3:c.2532G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*506G>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.723G>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.588G>C
  hgvsp: ENST00000338806.4:c.588G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1489G>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2532G>C
  hgvsp: ENST00000344733.5:c.2532G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1598G>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.558G>C
  hgvsp: ENST00000538395.1:c.558G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.987G>C
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22861
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser844Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

4-3418744-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418744
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418744
    reference: chr 4
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1489G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2532G>T
  hgvsp: ENST00000336727.3:c.2532G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1598G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.726G>T
  hgvsp: ENST00000306648.7:c.726G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.558G>T
  hgvsp: ENST00000538395.1:c.558G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2532G>T
  hgvsp: ENST00000382788.3:c.2532G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.723G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.813G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.588G>T
  hgvsp: ENST00000338806.4:c.588G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2532G>T
  hgvsp: ENST00000344733.5:c.2532G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.670G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.987G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*506G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*506G>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22861
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser844Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

4-3418750-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418750
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418750
    reference: chr 4
allele count: 1
allele frequency: 8.316146630297385e-6
allele num: 120248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.594G>T
  hgvsp: ENSP00000342133.4:p.Gln198His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2538G>T
  hgvsp: ENSP00000338509.3:p.Gln846His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1604G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*512G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.732G>T
  hgvsp: ENSP00000304459.7:p.Gln244His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*512G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.993G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.564G>T
  hgvsp: ENSP00000438888.1:p.Gln188His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1495G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.729G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2538G>T
  hgvsp: ENSP00000372238.3:p.Gln846His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2538G>T
  hgvsp: ENSP00000339381.5:p.Gln846His
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.676G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.819G>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18435
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln846His
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

4-3418755-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418755
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418755
    reference: chr 4
allele count: 2
allele frequency: 1.664170411050091e-5
allele num: 120180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1609C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2543C>G
  hgvsp: ENSP00000338509.3:p.Pro848Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.569C>G
  hgvsp: ENSP00000438888.1:p.Pro190Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*517C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.734C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2543C>G
  hgvsp: ENSP00000339381.5:p.Pro848Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2543C>G
  hgvsp: ENSP00000372238.3:p.Pro848Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.737C>G
  hgvsp: ENSP00000304459.7:p.Pro246Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.599C>G
  hgvsp: ENSP00000342133.4:p.Pro200Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.824C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1500C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.681C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*517C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.998C>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22787
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18418
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro848Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/4-3418759-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418759
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418759
    reference: chr 4
allele count: 3
allele frequency: 2.498584135656461e-5
allele num: 120068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*521C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2547C>A
  hgvsp: ENSP00000372238.3:p.Ser849Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.603C>A
  hgvsp: ENSP00000342133.4:p.Ser201Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.741C>A
  hgvsp: ENSP00000304459.7:p.Ser247Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2547C>A
  hgvsp: ENSP00000339381.5:p.Ser849Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1613C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.828C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1504C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.738C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.685C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2547C>A
  hgvsp: ENSP00000338509.3:p.Ser849Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*521C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.573C>A
  hgvsp: ENSP00000438888.1:p.Ser191Arg
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1002C>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser849Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

4-3418764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418764
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418764
    reference: chr 4
allele count: 4
allele frequency: 3.333833408344585e-5
allele num: 119982
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.578C>T
  hgvsp: ENSP00000438888.1:p.Pro193Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.743C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.608C>T
  hgvsp: ENSP00000342133.4:p.Pro203Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1509C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*526C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1007C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*526C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2552C>T
  hgvsp: ENSP00000338509.3:p.Pro851Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.746C>T
  hgvsp: ENSP00000304459.7:p.Pro249Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2552C>T
  hgvsp: ENSP00000372238.3:p.Pro851Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.690C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2552C>T
  hgvsp: ENSP00000339381.5:p.Pro851Leu
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1618C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.833C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro851Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

4-3418775-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418775
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418775
    reference: chr 4
allele count: 1
allele frequency: 8.365680631776201e-6
allele num: 119536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2563C>G
  hgvsp: ENSP00000372238.3:p.His855Asp
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.619C>G
  hgvsp: ENSP00000342133.4:p.His207Asp
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1018C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.757C>G
  hgvsp: ENSP00000304459.7:p.His253Asp
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2563C>G
  hgvsp: ENSP00000339381.5:p.His855Asp
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.701C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1629C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*537C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*537C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2563C>G
  hgvsp: ENSP00000338509.3:p.His855Asp
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.844C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.589C>G
  hgvsp: ENSP00000438888.1:p.His197Asp
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.754C>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1520C>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His855Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

4-3418783-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418783
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418783
    reference: chr 4
allele count: 1
allele frequency: 8.396869646995599e-6
allele num: 119092
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.852C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1637C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.765C>T
  hgvsp: ENST00000306648.7:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1528C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*545C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2571C>T
  hgvsp: ENST00000382788.3:c.2571C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.597C>T
  hgvsp: ENST00000538395.1:c.597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1026C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.762C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2571C>T
  hgvsp: ENST00000344733.5:c.2571C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.709C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2571C>T
  hgvsp: ENST00000336727.3:c.2571C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.627C>T
  hgvsp: ENST00000338806.4:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*545C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6336
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu857Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

4-3418784-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418784
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418784
    reference: chr 4
allele count: 1
allele frequency: 8.399408681628814e-6
allele num: 119056
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.628G>A
  hgvsp: ENSP00000342133.4:p.Gly210Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2572G>A
  hgvsp: ENSP00000338509.3:p.Gly858Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.598G>A
  hgvsp: ENSP00000438888.1:p.Gly200Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1529G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.710G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*546G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1027G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1638G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.853G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.763G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2572G>A
  hgvsp: ENSP00000372238.3:p.Gly858Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2572G>A
  hgvsp: ENSP00000339381.5:p.Gly858Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.766G>A
  hgvsp: ENSP00000304459.7:p.Gly256Ser
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*546G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly858Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-3418795-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418795
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418795
    reference: chr 4
allele count: 1
allele frequency: 8.459664320519762e-6
allele num: 118208
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2583C>A
  hgvsp: ENSP00000339381.5:p.His861Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.774C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1540C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.777C>A
  hgvsp: ENSP00000304459.7:p.His259Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*557C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.639C>A
  hgvsp: ENSP00000342133.4:p.His213Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2583C>A
  hgvsp: ENSP00000372238.3:p.His861Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1649C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.721C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2583C>A
  hgvsp: ENSP00000338509.3:p.His861Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.864C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1038C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*557C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.609C>A
  hgvsp: ENSP00000438888.1:p.His203Gln
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His861Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

4-3418802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418802
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418802
    reference: chr 4
allele count: 1
allele frequency: 8.538397172082857e-6
allele num: 117118
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.646G>A
  hgvsp: ENSP00000342133.4:p.Val216Met
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.728G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1045G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.784G>A
  hgvsp: ENSP00000304459.7:p.Val262Met
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2590G>A
  hgvsp: ENSP00000372238.3:p.Val864Met
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*564G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2590G>A
  hgvsp: ENSP00000339381.5:p.Val864Met
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1547G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*564G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2590G>A
  hgvsp: ENSP00000338509.3:p.Val864Met
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.616G>A
  hgvsp: ENSP00000438888.1:p.Val206Met
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1656G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.871G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.781G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1439
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val864Met
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

4-3418803-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418803
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418803
    reference: chr 4
allele count: 1
allele frequency: 8.552125203112974e-6
allele num: 116930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.729T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.785T>C
  hgvsp: ENSP00000304459.7:p.Val262Ala
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.647T>C
  hgvsp: ENSP00000342133.4:p.Val216Ala
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1046T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1548T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*565T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2591T>C
  hgvsp: ENSP00000338509.3:p.Val864Ala
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2591T>C
  hgvsp: ENSP00000339381.5:p.Val864Ala
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.782T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1657T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.617T>C
  hgvsp: ENSP00000438888.1:p.Val206Ala
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.872T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2591T>C
  hgvsp: ENSP00000372238.3:p.Val864Ala
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*565T>C
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val864Ala
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

4-3418804-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418804
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418804
    reference: chr 4
allele count: 1
allele frequency: 8.572800219463686e-6
allele num: 116648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1549G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1658G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.783G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.730G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*566G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2592G>A
  hgvsp: ENST00000336727.3:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.618G>A
  hgvsp: ENST00000538395.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2592G>A
  hgvsp: ENST00000382788.3:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2592G>A
  hgvsp: ENST00000344733.5:c.2592G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*566G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.648G>A
  hgvsp: ENST00000338806.4:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1047G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.786G>A
  hgvsp: ENST00000306648.7:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.873G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val864Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

4-3418806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418806
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418806
    reference: chr 4
allele count: 3
allele frequency: 2.580556367952931e-5
allele num: 116254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2594C>T
  hgvsp: ENSP00000338509.3:p.Ser865Phe
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*568C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1551C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.875C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1660C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2594C>T
  hgvsp: ENSP00000372238.3:p.Ser865Phe
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.788C>T
  hgvsp: ENSP00000304459.7:p.Ser263Phe
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2594C>T
  hgvsp: ENSP00000339381.5:p.Ser865Phe
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.732C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.785C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*568C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1049C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.650C>T
  hgvsp: ENSP00000342133.4:p.Ser217Phe
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.620C>T
  hgvsp: ENSP00000438888.1:p.Ser207Phe
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17561
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser865Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-3418810-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418810
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418810
    reference: chr 4
allele count: 5
allele frequency: 4.358513921093464e-5
allele num: 114718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2598G>A
  hgvsp: ENST00000382788.3:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.789G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2598G>A
  hgvsp: ENST00000344733.5:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.879G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.624G>A
  hgvsp: ENST00000538395.1:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2598G>A
  hgvsp: ENST00000336727.3:c.2598G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1053G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.654G>A
  hgvsp: ENST00000338806.4:c.654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*572G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1555G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.792G>A
  hgvsp: ENST00000306648.7:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*572G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.736G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1664G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19986
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr866Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff

4-3418826-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418826
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418826
    reference: chr 4
allele count: 1
allele frequency: 1.041644965729881e-5
allele num: 96002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+7T>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+7T>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5085
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2607+7T>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/4-3418827-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418827
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418827
    reference: chr 4
allele count: 1
allele frequency: 1.040539415633064e-5
allele num: 96104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+8C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+8C>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2607+8C>A
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

4-3418830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418830
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418830
    reference: chr 4
allele count: 3
allele frequency: 3.244295447172056e-5
allele num: 92470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+11C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+11C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

4-3418831-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418831
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418831
    reference: chr 4
allele count: 5
allele frequency: 5.406925189783074e-5
allele num: 92474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+12G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+12G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21953
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/4-3418842-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418842
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418842
    reference: chr 4
allele count: 8
allele frequency: 9.653674429829854e-5
allele num: 82870
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+23C>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+23C>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25712
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

4-3418844-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418844
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418844
    reference: chr 4
allele count: 2
allele frequency: 2.476044271671578e-5
allele num: 80774
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+25C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+25C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25601
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15936
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

4-3418867-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418867
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418867
    reference: chr 4
allele count: 1
allele frequency: 1.536806516059628e-5
allele num: 65070
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+48C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+48C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21988
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

4-3418870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3418870
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3418870
    reference: chr 4
allele count: 1
allele frequency: 1.564015139666552e-5
allele num: 63938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.633+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.798+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2607+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.801+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*581+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2607+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.745+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*581+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.663+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1673+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2607+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.888+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1062+51C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1564+51C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8031
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum

4-3419071-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419071
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419071
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 95774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.889-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2608-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*582-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.802-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2608-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2608-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1565-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.664-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1063-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1674-26A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.634-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.799-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.746-44A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*582-44A>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 14365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP

4-3419082-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419082
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419082
    reference: chr 4
allele count: 14
allele frequency: 1.44234731723399e-4
allele num: 97064
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.664-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.746-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.799-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2608-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1674-15A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*582-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2608-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.802-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1565-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2608-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1063-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*582-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.889-33A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.634-33A>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25625
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

4-3419093-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419093
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419093
    reference: chr 4
allele count: 817
allele frequency: 8.118044515103338e-3
allele num: 100640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.802-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.664-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.799-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.746-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2608-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1674-4C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2608-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1063-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.634-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*582-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2608-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*582-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1565-22C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.889-22C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 3.25e1
  variant carriers: 101
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33903
  bin: 2.25e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 7.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 2.75e1
  variant carriers: 218
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 3.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.1674-4C>T
num of homozygotes: 16
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

4-3419094-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419094
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419094
    reference: chr 4
allele count: 1
allele frequency: 9.854352667573266e-6
allele num: 101478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*582-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2608-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.889-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1674-3A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2608-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2608-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.746-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1063-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.799-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.634-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1565-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.802-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.664-21A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*582-21A>G
  variant of: http://identifiers.org/hgnc/9994
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: n.1674-3A>G
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

4-3419110-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419110
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419110
    reference: chr 4
allele count: 3
allele frequency: 2.794024512908393e-5
allele num: 107372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.802-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2608-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2608-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.889-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2608-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.746-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.799-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1063-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.664-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.634-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1565-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*582-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*582-5G>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1687G>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39558
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1755
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2608-5G>T
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: DP

4-3419112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419112
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419112
    reference: chr 4
allele count: 1
allele frequency: 9.258916336431984e-6
allele num: 108004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2608-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2608-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.802-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1689C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2608-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.799-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*582-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.664-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*582-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.634-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1565-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.746-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1063-3C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.889-3C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2608-3C>T
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

4-3419125-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419125
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419125
    reference: chr 4
allele count: 1
allele frequency: 8.97778895013736e-6
allele num: 111386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.899A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2618A>T
  hgvsp: ENSP00000338509.3:p.Lys873Ile
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*592A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.809A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1575A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.674A>T
  hgvsp: ENSP00000342133.4:p.Lys225Ile
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2618A>T
  hgvsp: ENSP00000339381.5:p.Lys873Ile
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1073A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*592A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.812A>T
  hgvsp: ENSP00000304459.7:p.Lys271Ile
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.644A>T
  hgvsp: ENSP00000438888.1:p.Lys215Ile
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2618A>T
  hgvsp: ENSP00000372238.3:p.Lys873Ile
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.756A>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1702A>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4630
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10739
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys873Ile
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

4-3419135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419135
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419135
    reference: chr 4
allele count: 3
allele frequency: 2.64844536257217e-5
allele num: 113274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.909C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.654C>T
  hgvsp: ENST00000538395.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.766C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1712C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*602C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.822C>T
  hgvsp: ENST00000306648.7:c.822C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2628C>T
  hgvsp: ENST00000344733.5:c.2628C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.684C>T
  hgvsp: ENST00000338806.4:c.684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2628C>T
  hgvsp: ENST00000382788.3:c.2628C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2628C>T
  hgvsp: ENST00000336727.3:c.2628C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*602C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1585C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.819C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1083C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser876Ser
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

4-3419139-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419139
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419139
    reference: chr 4
allele count: 1
allele frequency: 8.717787774174425e-6
allele num: 114708
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.770C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.823C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1087C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.688C>T
  hgvsp: ENSP00000342133.4:p.Arg230Ter
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*606C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1716C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.658C>T
  hgvsp: ENSP00000438888.1:p.Arg220Ter
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*606C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2632C>T
  hgvsp: ENSP00000339381.5:p.Arg878Ter
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2632C>T
  hgvsp: ENSP00000338509.3:p.Arg878Ter
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.826C>T
  hgvsp: ENSP00000304459.7:p.Arg276Ter
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2632C>T
  hgvsp: ENSP00000372238.3:p.Arg878Ter
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.913C>T
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1589C>T
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg878Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-3419140-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419140
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419140
    reference: chr 4
allele count: 1
allele frequency: 8.667163584045485e-6
allele num: 115378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1590G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2633G>A
  hgvsp: ENSP00000338509.3:p.Arg878Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2633G>A
  hgvsp: ENSP00000372238.3:p.Arg878Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*607G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.771G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1717G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.827G>A
  hgvsp: ENSP00000304459.7:p.Arg276Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.824G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.689G>A
  hgvsp: ENSP00000342133.4:p.Arg230Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.659G>A
  hgvsp: ENSP00000438888.1:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1088G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2633G>A
  hgvsp: ENSP00000339381.5:p.Arg878Gln
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.914G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*607G>A
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11895
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41897
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg878Gln
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

4-3419146-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419146
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419146
    reference: chr 4
allele count: 3
allele frequency: 2.573914237177617e-5
allele num: 116554
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.777T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.695T>C
  hgvsp: ENSP00000342133.4:p.Leu232Pro
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2639T>C
  hgvsp: ENSP00000372238.3:p.Leu880Pro
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.830T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1596T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2639T>C
  hgvsp: ENSP00000338509.3:p.Leu880Pro
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.665T>C
  hgvsp: ENSP00000438888.1:p.Leu222Pro
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.833T>C
  hgvsp: ENSP00000304459.7:p.Leu278Pro
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1723T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.920T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2639T>C
  hgvsp: ENSP00000339381.5:p.Leu880Pro
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*613T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1094T>C
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*613T>C
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42382
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu880Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

4-3419147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419147
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419147
    reference: chr 4
allele count: 2
allele frequency: 1.713561122725248e-5
allele num: 116716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.831G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.696G>A
  hgvsp: ENST00000338806.4:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2640G>A
  hgvsp: ENST00000382788.3:c.2640G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.834G>A
  hgvsp: ENST00000306648.7:c.834G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1597G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.666G>A
  hgvsp: ENST00000538395.1:c.666G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1095G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*614G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*614G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.921G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1724G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2640G>A
  hgvsp: ENST00000336727.3:c.2640G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.778G>A
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2640G>A
  hgvsp: ENST00000344733.5:c.2640G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu880Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

4-3419153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3419153
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 3419153
    reference: chr 4
allele count: 2
allele frequency: 1.704622937406246e-5
allele num: 117328
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000424251
  ensembl transcript: ENST00000514268
  gene symbol: RGS12
  hgvsc: ENST00000514268.1:c.*620A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000508158
  gene symbol: RGS12
  hgvsc: ENST00000508158.1:n.927A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506631
  gene symbol: RGS12
  hgvsc: ENST00000506631.1:n.837A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000304459
  ensembl transcript: ENST00000306648
  gene symbol: RGS12
  hgvsc: ENST00000306648.7:c.840A>G
  hgvsp: ENST00000306648.7:c.840A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000338509
  ensembl transcript: ENST00000336727
  gene symbol: RGS12
  hgvsc: ENST00000336727.3:c.2646A>G
  hgvsp: ENST00000336727.3:c.2646A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000512266
  gene symbol: RGS12
  hgvsc: ENST00000512266.1:n.1730A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000339381
  ensembl transcript: ENST00000344733
  gene symbol: RGS12
  hgvsc: ENST00000344733.5:c.2646A>G
  hgvsp: ENST00000344733.5:c.2646A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000506998
  gene symbol: RGS12
  hgvsc: ENST00000506998.1:n.784A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000440566
  ensembl transcript: ENST00000543385
  gene symbol: RGS12
  hgvsc: ENST00000543385.1:c.*620A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000342133
  ensembl transcript: ENST00000338806
  gene symbol: RGS12
  hgvsc: ENST00000338806.4:c.702A>G
  hgvsp: ENST00000338806.4:c.702A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000372238
  ensembl transcript: ENST00000382788
  gene symbol: RGS12
  hgvsc: ENST00000382788.3:c.2646A>G
  hgvsp: ENST00000382788.3:c.2646A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000159788
  ensembl protein: ENSP00000438888
  ensembl transcript: ENST00000538395
  gene symbol: RGS12
  hgvsc: ENST00000538395.1:c.672A>G
  hgvsp: ENST00000538395.1:c.672A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000504194
  gene symbol: RGS12
  hgvsc: ENST00000504194.1:n.1603A>G
  variant of: http://identifiers.org/hgnc/9994
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000159788
  ensembl transcript: ENST00000513991
  gene symbol: RGS12
  hgvsc: ENST00000513991.1:n.1101A>G
  variant of: http://identifiers.org/hgnc/9994
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu882Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

GenotypeDepth
all individuals: 161
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3866
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 323
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 708
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1389
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6071
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3188
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11189
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5734
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4781
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4468
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5239
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10872
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.023122570083896e-4
allele num: 9774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6122
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.832e0

VQSLOD
type: SiteQuality
SIO_000300: -4.787e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 9.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.54e-1

DP
type: SiteQuality
SIO_000300: 1.360064e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e0

GenotypeDepth
all individuals: 6399
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 23
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 13
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 363
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 41
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 21268
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2607
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8758
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 578
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.707767328456984e-5
allele num: 11484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 9.710623422023694e-5
allele num: 10298
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: 11
allele frequency: 1.72538193681965e-4
allele num: 63754
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.682245e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.011e0

MQRankSum
type: SiteQuality
SIO_000300: 5.77e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

QD
type: SiteQuality
SIO_000300: 1.297e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeDepth
all individuals: 1534
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 592
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1650
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18329
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40005
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8759
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 528
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2817
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10136
num of homozygotes: 0

European (Finnish)
type: Population
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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BaseQRankSum
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FS
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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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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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 2.507208223642973e-4
allele num: 63816
num of homozygotes: 0

African
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allele frequency: 9.850275807722617e-5
allele num: 10152
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Latino
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Other
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South Asian
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East Asian
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ClippingRankSum
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DP
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FS
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MQRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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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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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 1.971220185294697e-4
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South Asian
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East Asian
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Other
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Latino
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European (Non-Finnish)
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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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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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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allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

African
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Other
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South Asian
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allele count: 0
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Latino
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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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VQSLOD
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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DP
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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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African
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Other
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European (Non-Finnish)
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East Asian
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FS
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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DP
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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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South Asian
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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FS
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MQ
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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Latino
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African
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European (Finnish)
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MQ
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ReadPosRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 3.478664192949907e-4
allele num: 8624
num of homozygotes: 0

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

East Asian
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allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535013661621589e-5
allele num: 65146
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65692
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Latino
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East Asian
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 3

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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European (Non-Finnish)
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allele count: 4
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allele num: 65968
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East Asian
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African
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Other
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European (Finnish)
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Latino
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South Asian
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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FS
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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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Other
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African
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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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MQ
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VQSLOD
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QD
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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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African
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Other
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Latino
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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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MQRankSum
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QD
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BaseQRankSum
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DP
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FS
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MQ
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ReadPosRankSum
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ClippingRankSum
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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: 11568
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66226
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.928640308582449e-4
allele num: 10370
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.156e0

BaseQRankSum
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SIO_000300: -5.374e0

MQ
type: SiteQuality
SIO_000300: 5.998e1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.777315e6

VQSLOD
type: SiteQuality
SIO_000300: 5.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
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SIO_000300: 1.04e0

ReadPosRankSum
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SIO_000300: 1.04e0

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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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: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.532543663503958e-5
allele num: 66188
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.23e1

VQSLOD
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SIO_000300: 2.88e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

FS
type: SiteQuality
SIO_000300: 5.31e-1

DP
type: SiteQuality
SIO_000300: 1.776586e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.54e-1

ClippingRankSum
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SIO_000300: -1.308e0

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 17

GenotypeDepth
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variant carriers: 12

GenotypeDepth
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variant carriers: 9

GenotypeDepth
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variant carriers: 11

GenotypeDepth
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variant carriers: 9

GenotypeDepth
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 267

GenotypeQuality
all individuals: 574
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variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 12
allele frequency: 1.038421599169263e-3
allele num: 11556
num of homozygotes: 0

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

African
type: Population
allele count: 234
allele frequency: 2.258687258687259e-2
allele num: 10360
num of homozygotes: 2

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

European (Non-Finnish)
type: Population
allele count: 20
allele frequency: 3.022974607013301e-4
allele num: 66160
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.832620647525962e-4
allele num: 16370
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.782592e6

FS
type: SiteQuality
SIO_000300: 5.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

BaseQRankSum
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SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.417e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 4
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.104260774020266e-5
allele num: 16382
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66110
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2376e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

InbreedingCoeff
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SIO_000300: -5.0e-4

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 1.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.34e-1

DP
type: SiteQuality
SIO_000300: 1.767579e6

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66108
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.104260774020266e-5
allele num: 16382
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.515e1

ReadPosRankSum
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SIO_000300: 1.16e0

VQSLOD
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SIO_000300: 8.49e-1

ClippingRankSum
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SIO_000300: -1.202e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -4.0e-4

FS
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BaseQRankSum
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MQRankSum
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SIO_000300: 6.57e-1

DP
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SIO_000300: 1.767403e6

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514004542013626e-5
allele num: 66050
num of homozygotes: 0

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

GenotypeQuality
all individuals: 205
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513867021920794e-5
allele num: 66056
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.222e1

InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
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MQRankSum
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DP
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ClippingRankSum
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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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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 4.330504070673827e-4
allele num: 11546
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele num: 65998
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African
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East Asian
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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ReadPosRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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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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Latino
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East Asian
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European (Non-Finnish)
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African
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allele num: 10332
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South Asian
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European (Finnish)
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ReadPosRankSum
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BaseQRankSum
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MQ
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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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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European (Finnish)
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Other
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East Asian
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South Asian
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African
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European (Non-Finnish)
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BaseQRankSum
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 6598
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Latino
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European (Non-Finnish)
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South Asian
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African
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East Asian
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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MQ
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DP
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MQRankSum
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FS
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ReadPosRankSum
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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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European (Finnish)
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Other
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Latino
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South Asian
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East Asian
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African
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European (Non-Finnish)
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DP
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InbreedingCoeff
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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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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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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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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.516254245511887e-5
allele num: 65952
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

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

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 1.35e0

ReadPosRankSum
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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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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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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FS
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DP
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SIO_000300: 1.762064e6

MQRankSum
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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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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.516254245511887e-5
allele num: 65952
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
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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

FS
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
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QD
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SIO_000300: 1.385e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.516944267467613e-5
allele num: 65922
num of homozygotes: 0

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

East Asian
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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
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.645e0

DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 5.88e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeDepth
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bin: 5.25e1
variant carriers: 1

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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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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bin: 2.25e1
variant carriers: 0

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

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

Other
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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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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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num of homozygotes: 0

South Asian
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MQ
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ReadPosRankSum
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VQSLOD
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FS
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: 2.01e0

MQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

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

South Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65806
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African
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Latino
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East Asian
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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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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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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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variant carriers: 4

European (Finnish)
type: Population
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European (Non-Finnish)
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African
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East Asian
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South Asian
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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South Asian
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European (Non-Finnish)
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.529987760097919e-5
allele num: 65360
num of homozygotes: 0

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

South Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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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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MQ
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MQRankSum
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InbreedingCoeff
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DP
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FS
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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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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South Asian
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East Asian
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Other
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African
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European (Non-Finnish)
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Latino
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European (Finnish)
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InbreedingCoeff
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DP
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QD
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MQ
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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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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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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Latino
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African
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InbreedingCoeff
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FS
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MQ
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QD
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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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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Latino
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European (Non-Finnish)
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East Asian
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FS
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ClippingRankSum
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MQ
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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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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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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allele frequency: 6.65513110608279e-5
allele num: 15026
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQ
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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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: 10022
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.668388783417883e-5
allele num: 64262
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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QD
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MQ
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BaseQRankSum
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FS
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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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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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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allele count: 4
allele frequency: 3.555555555555556e-4
allele num: 11250
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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FS
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ReadPosRankSum
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MQ
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QD
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MQRankSum
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InbreedingCoeff
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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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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 (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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African
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European (Non-Finnish)
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Other
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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DP
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QD
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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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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
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South Asian
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East Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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MQ
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QD
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FS
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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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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European (Non-Finnish)
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allele num: 51954
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European (Finnish)
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Latino
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Other
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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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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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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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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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variant carriers: 0

African
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allele frequency: 2.424242424242424e-4
allele num: 8250
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6718
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 5.778565374836274e-5
allele num: 51916
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5046
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -5.8e-3

FS
type: SiteQuality
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VQSLOD
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DP
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QD
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 8
allele frequency: 8.410428931875525e-4
allele num: 9512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5926
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47058
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.36e-1

MQRankSum
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MQ
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VQSLOD
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FS
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -9.4e-3

DP
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SIO_000300: 7.99375e5

QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.965e0

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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bin: 3.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7382
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.353125544140693e-5
allele num: 45944
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5768
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.684e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

DP
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SIO_000300: 7.77141e5

MQRankSum
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: 2.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
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SIO_000300: 6.0e1

GenotypeDepth
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bin: 7.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6134
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3826
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4394
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.645782622499736e-5
allele num: 37796
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

DP
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ClippingRankSum
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SIO_000300: -9.05e-1

VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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SIO_000300: -3.223e0

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 7.14e0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.691065662002153e-5
allele num: 37160
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 5332
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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DP
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ReadPosRankSum
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6006
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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South Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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FS
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VQSLOD
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MQ
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
allele frequency: 4.676174888940846e-4
allele num: 8554
num of homozygotes: 0

Latino
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allele count: 5
allele frequency: 4.942665085013839e-4
allele num: 10116
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6054
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 5.352936978088645e-5
allele num: 56044
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.72108843537415e-4
allele num: 7350
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.576e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 2.799e0

QD
type: SiteQuality
SIO_000300: 1.36e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.69e-1

DP
type: SiteQuality
SIO_000300: 1.038712e6

GenotypeDepth
all individuals: 5
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1456
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variant carriers: 132

GenotypeDepth
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variant carriers: 59

GenotypeDepth
all individuals: 8
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variant carriers: 2

GenotypeDepth
all individuals: 4
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variant carriers: 4

GenotypeDepth
all individuals: 17
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variant carriers: 4

GenotypeQuality
all individuals: 1323
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variant carriers: 3

GenotypeQuality
all individuals: 464
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variant carriers: 2

GenotypeQuality
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bin: 2.5e0
variant carriers: 1

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 1962
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variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 8413
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 80
bin: 9.25e1
variant carriers: 6

GenotypeQuality
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bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 307
bin: 1.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 471
bin: 5.25e1
variant carriers: 4

GenotypeQuality
all individuals: 969
bin: 9.75e1
variant carriers: 788

African
type: Population
allele count: 5
allele frequency: 5.640794223826715e-4
allele num: 8864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.558063845994045e-4
allele num: 57764
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 4.098360655737705e-3
allele num: 732
num of homozygotes: 0

South Asian
type: Population
allele count: 133
allele frequency: 1.508620689655172e-2
allele num: 8816
num of homozygotes: 4

Latino
type: Population
allele count: 477
allele frequency: 4.505100113335852e-2
allele num: 10588
num of homozygotes: 9

East Asian
type: Population
allele count: 190
allele frequency: 2.466891716437289e-2
allele num: 7702
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.153653e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

QD
type: SiteQuality
SIO_000300: 1.37e1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
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variant carriers: 0

GenotypeDepth
all individuals: 2
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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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GenotypeQuality
all individuals: 2539
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 187
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variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.718567402213515e-5
allele num: 58188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

VQSLOD
type: SiteQuality
SIO_000300: -1.914e0

FS
type: SiteQuality
SIO_000300: 7.636e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

MQ
type: SiteQuality
SIO_000300: 5.873e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.366e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.224e0

DP
type: SiteQuality
SIO_000300: 1.163025e6

QD
type: SiteQuality
SIO_000300: 9.56e0

GenotypeDepth
all individuals: 1
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variant carriers: 0

GenotypeDepth
all individuals: 6311
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variant carriers: 0

GenotypeDepth
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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
all individuals: 2
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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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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 481
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.633133002351711e-5
allele num: 61232
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8252
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.78826895565093e-4
allele num: 11184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10022
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

QD
type: SiteQuality
SIO_000300: 1.207e1

FS
type: SiteQuality
SIO_000300: 1.855e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.001e0

DP
type: SiteQuality
SIO_000300: 1.257961e6

GenotypeDepth
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
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variant carriers: 0

GenotypeDepth
all individuals: 9664
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 8
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GenotypeQuality
all individuals: 160
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GenotypeQuality
all individuals: 79
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GenotypeQuality
all individuals: 45443
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 229
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GenotypeQuality
all individuals: 309
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.846396218983852e-5
allele num: 10156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61588
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.267396e6

VQSLOD
type: SiteQuality
SIO_000300: -1.477e0

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.438e0

FS
type: SiteQuality
SIO_000300: 7.439e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.112e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.21e-1

QD
type: SiteQuality
SIO_000300: 9.66e0

MQ
type: SiteQuality
SIO_000300: 5.898e1

GenotypeDepth
all individuals: 40758
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 32
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GenotypeDepth
all individuals: 2
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GenotypeDepth
all individuals: 1
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GenotypeDepth
all individuals: 7
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GenotypeDepth
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GenotypeQuality
all individuals: 31
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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: 221
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62980
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.30597e6

QD
type: SiteQuality
SIO_000300: 1.609e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

FS
type: SiteQuality
SIO_000300: 6.058e0

VQSLOD
type: SiteQuality
SIO_000300: -2.653e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.456e0

ReadPosRankSum
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SIO_000300: 3.13e0

MQ
type: SiteQuality
SIO_000300: 5.267e1

MQRankSum
type: SiteQuality
SIO_000300: -1.653e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.788e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 3
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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
all individuals: 62
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 737
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GenotypeQuality
all individuals: 186
bin: 9.75e1
variant carriers: 3

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.001201441730076e-4
allele num: 9988
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.14099946603009e-5
allele num: 63674
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

BaseQRankSum
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.329813e6

QD
type: SiteQuality
SIO_000300: 1.205e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 7.632422530911312e-5
allele num: 13102
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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Other
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East Asian
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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FS
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MQ
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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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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South Asian
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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 count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64352
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.529987760097919e-4
allele num: 6536
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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ReadPosRankSum
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SIO_000300: -1.07e-1

MQ
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SIO_000300: 5.964e1

VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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FS
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SIO_000300: 4.754e0

QD
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BaseQRankSum
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SIO_000300: 1.2e-1

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

South Asian
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allele frequency: 1.401738155312588e-4
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.545881770962157e-5
allele num: 64688
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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SIO_000300: 5.92e0

ReadPosRankSum
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SIO_000300: -2.14e-1

ClippingRankSum
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MQ
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SIO_000300: 5.944e1

MQRankSum
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SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.36227e6

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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Other
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 64730
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African
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allele count: 0
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Latino
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South Asian
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MQ
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QD
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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SIO_000300: 2.2e-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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

East Asian
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African
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allele count: 0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
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allele num: 64908
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Other
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South Asian
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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BaseQRankSum
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FS
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ClippingRankSum
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DP
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